The Remnant Online
Health => Healthful Living => Recalls => Topic started by: Mimi on March 09, 2009, 04:30:16 PM
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FDA Warns Consumers About Potentially Contaminated Cheese
Mon, 09 Mar 2009 17:24:00 -0500
The U.S. Food and Drug Administration is warning consumers not to eat Queso Fresco Fresh Cheese Mexican style soft cheese (two specific lots) or any Queso Cotija Molido Mexican style grated cheese manufactured and distributed by Peregrina Cheese Corp. of New York City. These products could be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in pregnant women, young children, frail or elderly people, and others with weakened immune systems.
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Sad! But, Seventh-day Adventists are protected from this one because we were told over a hundred years ago to not eat one bite of cheese even when milk was still safe to drink.
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Torres Hillsdale Country Cheese LLC Expands the Recall of Asadero and Oaxaca Cheeses due to Possible Listeria Contamination
Contact:
Salvador Torres, Manager
517-368-5990
FOR IMMEDIATE RELEASE -- March 23, 2009 -- Torres Hillsdale Country Cheese of Reading, Michigan is expanding the recall of Asadero and Oaxaca soft Mexican-style cheeses due to potential Listeria contamination.
Consumption of food contaminated with Listeria monocytogenes can cause Listeriosis, an uncommon but potentially fatal disease. Listeriosis can cause high fever, severe headache, neck stiffness and nausea. Listeriosis can also cause miscarriages and stillbirths. The very young, the pregnant, the elderly and persons with compromised immune systems are the most susceptible to infection. People experiencing these problems should seek immediate medical attention.
Products were distributed to the following states: Illinois, Indiana, Michigan, Georgia, Tennessee, Kentucky, North Carolina, South Carolina, Ohio, Wisconsin, New Jersey, Pennsylvania, Florida, and Alabama.
A routine sample of Asadero cheese, taken by an inspector from the Michigan Department of Agriculture’s Food and Dairy Division on February 23, 2009, was subsequently tested by the Michigan Department of Agriculture Laboratory and discovered to be contaminated with Listeria monocytogenes.
The recalled Asadero and Oaxaca cheese products were distributed to retails stores and delis in 10 lb balls, 16- and 12 oz plastic packages, sold under the name "Aguas Calientes". Product was also sold in 6 lb blocks shrink-wrapped in clear plastic, under the name "El Jaliciense". Packaging may also include a label with the name "Torres Hillsdale Country Cheese LLC".
The recall encompasses all productions dates between August 1, 2008 (expiration date 10/29/2008) and February 27, 2009 (expiration date 5/10/2009).
No illnesses have been reported to date in connection with the recalled products.
Consumers and retailers are urged to return all unused recalled product to the manufacturer.
Consumers with questions may contact Salvador Torres, Manager, Torres Hillsdale Country Cheese LLC at 517-368-5990.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Torres Hillsdale Country Cheese LLC Announces the Recall of all lots of Soft Mexican Cheeses due to Possible Listeria Contamination
Contact:
Salvador Torres, Manager
517-368-5990
FOR IMMEDIATE RELEASE -- June 13, 2009 - Torres Hillsdale Country Cheese of Reading, Michigan announces the recall of all lots of various types of soft Mexican-style cheeses due to potential Listeria contamination. Consumption of food contaminated with Listeria monocytogenes can cause Listeriosis, an uncommon but potentially fatal disease. Listeriosis can cause high fever, severe headache, neck stiffness and nausea. Listeriosis can also cause miscarriages and stillbirths. The very young, the pregnant, the elderly and persons with compromised immune systems are the most susceptible to infection. People experiencing these problems should seek immediate medical attention.
A sample of queso fresco cheese, taken by an investigator from the U.S. Food and Drug Administration on May 26, 2009, was subsequently tested by an FDA laboratory and discovered to be contaminated with Listeria monocytogenes.
The products were distributed to retails stores and delis in the following states: Illinois, Indiana, Michigan, Georgia, Tennessee, Kentucky, North Carolina, South Carolina, Ohio and Wisconsin.
The products were sold under the name 'Aguas Calientes' as follows:
Product Unit Size
Queso Asadero 12 oz and 10 lb ball
Queso Oaxaca 10 lb ball
Queso Fresco 1 lb and 8 oz.
Queso Requeson 1 gallon pail and 3 gallon pail
Morral Adobera 3 lb packages
Packaging may also include a label with the name "Torres Hillsdale Country Cheese LLC". The recall encompasses all expiration dates.
No illnesses have been reported to date in connection with the recalled products.
Consumers and retailers are urged to return all unused recalled product to the manufacturer. Consumers with questions may contact Salvador Torres, Manager, Torres Hillsdale Country Cheese LLC at 517-368-5990, Monday through Friday between 7 a.m. and 3 p.m. EDT.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Lancaster Foods, LLC Voluntarily Recalls Fresh Spinach with Best Enjoyed By Dates of June 19 to June 27, 2010 Due to Possible Health Risk
Contact:
Douglas Verner 703-849-9386
FOR IMMEDIATE RELEASE – June 24, 2010 – Jessup, Maryland – Lancaster Foods, LLC is voluntarily recalling fresh Spinach with the Best Enjoyed By dates of 19 JUN 10 through 27 JUN 10 sold under the brand names Krisp-Pak, Lancaster Fresh, Giant, and America's Choice because they could be contaminated with Listeria monocytogenes. The recall extends only to products with this Use-by Date or Product Code and sold in the following states: New Jersey, Delaware, Pennsylvania, Maryland, North Carolina, and Virginia. No other Lancaster Foods, LLC products are included in the recall.
The recall notification is being issued out of an abundance of caution based on a random sample test conducted by the North Carolina Department of Agriculture Food & Drug Protection Division (NCAGR) on fresh Spinach with the Best Enjoyed By dates of 23 JUN 10 sold under the brand name Krisp-Pak that was confirmed positive for Listeria monocytogenes in NCAGR labs. No illnesses have been associated with this possible contamination.
Although healthy individuals may suffer only short-term symptoms such as high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea, Listeria M. infection can cause serious and sometimes fatal infections in young children, frail, or elderly people, and others with weakened immune systems. It can also cause miscarriages and stillbirths among pregnant women. Consumers with any of these symptoms should consult their health care provider.
Because it is still possible that the spinach with the Best Enjoyed By dates of 19 JUN 10 through 27 JUN 10 sold under the brand names Krisp-Pak, Lancaster Fresh, Giant or America's Coice could be on store shelves, this recall extends to retailers as well as consumers. Lancaster Foods, LLC believes that it is important to alert consumers who might still possess one of the potentially affected expired packages of spinach to immediately dispose of it.
Spinach included in the recall notification includes the items listed in the table below with Best Enjoyed By dates of 19 JUN 10 through 27 JUN 10.
Instructions for Consumers:
Check your refrigerator for packaged fresh Spinach with the Best Enjoyed By dates of 19 JUN 10 through 27 JUN 10 sold under the brand name Krisp-Pak, Lancaster Fresh, Giant, or America's Choice. The Use-by Date is found on the front of the package in the upper right hand corner.
Consumers who may have potentially affected product are asked to empty the contents of the package into your garbage, save the package, and contact a Lancaster Foods, LLC consumer representative toll-free at (800) 247-8125 between the hours of 8:00 am to 5:00 pm.
Instructions for Retailers:
All Product Codes indicated expire between June 19, 2010 and June 27, 2010, inclusive, however, retailers are asked to reconfirm with their distribution centers and all individual stores to ensure that no product remains in their inventory or at store locations. A separate letter and instructions will be forwarded to all relevant Lancaster Foods, LLC customers. For additional details, retailers are asked to contact their Lancaster Foods, LLC customer service representative.
Complete Listing of Recalled Lancaster Foods, LLC spinach packed under the Krisp-Pac, Lancaster Fresh, Giant, and America's Choice brands, Use-by Dates and Product Codes.
Bag UPC Code Product Description Oz
33383 65201 Krisp-Pak Hydro-Cooled Fresh Spinach, Best Enjoyed by 19 JUN 10 thru 27 Jun 10 10 oz
13055 01145 Lancaster Fresh, Triple Washed, All Natural, Curly Leaf Spinach, Best Enjoyed by 19 JUN 10 thru 27 JUN 10 8, 10, and 12 oz
88267 09813 Giant, Fresh Spinach, Best Enjoyed by 19 JUN 10 thru 27 JUN 10 10 oz
54807 76060 America's Choice, Spinach, Cold Water Washed, Best Enjoyed by 19 Jun 10 thru 27 Jun 10 oz
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
J. Hellman Frozen Foods, Inc. Recalls Señor Mexicano™ Avocado Pulp Due to Possible Health Risk
Contact:
Greg Abadjian/213‐243‐9105
FOR IMMEDIATE RELEASE -- July 8, 2010 – J. Hellman Frozen Foods, Inc. of Los Angeles, CA is recalling 992 cases (4,960 retail units) of Señor Mexicano™ Avocado Pulp, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short‐term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Señor Mexicano™ Avocado Pulp was distributed in California and Hawaii. Dates and Product Codes as follows: Señor Mexicano™ Avocado Pulp, 2lbs bags (UPC Code 7 503012 650001) with the following Lot number: A 21 04 10 / A 21 04 12.
There have been no illnesses reported in accordance with this recall.
J. Hellman Frozen Foods, Inc. is collaborating with the FDA. This recall notification is being issued out of an abundance of caution based on a confirmed positive result for Listeria monocytogenes in a random sample test conducted by the FDA.
We have notified all of our customers who have received the product in question and have directed them to remove it from their shelves and return to us as soon as possible. Because it is possible that products bearing the Lot number A 21 04 10 / A 21 04 12 were further distributed and could be on store shelves and in consumer homes, this recall is being extended to the general public.
We are confident in our safety program and committed to continuing a safe supply of ready to use frozen avocado pulp.
Any Questions or comments please call Greg Abadjian, Director of Food Safety at 213‐243‐9105 between the hours of 4 A.M. to 9:30 A.M.
Instructions for Consumers:
Check your refrigerator/freezers for Señor Mexicano™ Avocado Pulp with the above Lot number. The Lot number can be found on a sticker affixed to the package. Consumers who have the affected product are asked to record the Lot number, and immediately dispose of the product or return to place of purchase for a refund.
Instructions for Retailers/Distributors:
Immediately examine your inventory and quarantine product subject to recall. If you have product purchased between these dates, please with the affected Lot number contact us immediately and return this product as soon as possible in order to credit your account accordingly.
Please identify your customers and notify them at once of this product recall. Your notification to your customers may include a copy of this recall notification.
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Florida Company Recalls Sliced Apples
Contact:
Ph: 813-752-3482
Fax: 813-754-4974
FOR IMMEDIATE RELEASE - On July 5, 2010 - Marjon Specialty Foods, Inc., Plant City, FL voluntarily recalled 119 cases of sliced apples as a result of a positive test result for Listeria monocytogenes that came from the company's routine sampling program. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant women.
No other products manufactured or distributed by Marjon Specialty Foods, Inc. are involved in this recall.
These apples were produced by Marjon Specialty Foods, Inc. and packaged in 2 oz. single serve packages which were labeled as follows:
http://www.fda.gov/Safety/Recalls/ucm218714.htm
This recall only extends to the products as shown above. They were sold to three foodservice distributors in Florida. This product was further distributed to institutional and food service establishments, where it may have been removed from its original packaging. These products have been successfully accounted for and destroyed by our customers.
No illnesses related to these products have been reported.
Marjon Specialty Foods, Inc. has worked closely with the Florida Department of Agriculture and Consumer Services (FDACS). Production was ceased immediately until FDACS was able to conduct and complete their inspection of the facility on July 6, 2010. Marjon has completed all of the requirements per FDACS guidelines. FDACS gave Marjon Specialty Foods, Inc. the release to resume production on Tuesday, July 6, 2010.
Marjon Specialty Foods, Inc. took immediate precautionary measures to protect public health by issuing this voluntary recall and requested that the three distributors involved locate, recall, and destroy all product involved in this recall. The distributors acted promptly to gather the product being recalled.
For additional details, please contact Marjon Specialty Foods, Inc. at 813-752-3482, M-F 8:00 AM to 4:00 PM EST.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Specialty Farms, LLC Recalls Organic Alfalfa Sprouts Blend and Organic Sprout Salad in the North Eastern United States Because of Possible Health Risk
Contact:
Specialty-Farms, LLC
(203) 366-6919
FOR IMMEDIATE RELEASE - July 23, 2010 - Specialty-Farms, LLC is voluntarily recalling Specialty Farms brand Organic Alfalfa Sprouts Blend and Organic Sprout Salad, as noted below. These items both have a "sell-by date of 7/26/2010" and are net weight 4 ounces in plastic containers:
BRAND ITEM DESCRIPTION UPC
Specialty Farms Organic Alfalfa Sprouts Blend 8192400108
Specialty Farms Organic Sprout Salad 8192400024
These sprouts are being recalled because they may have the potential to be contaminated with Listeria Monocytogenes (Lm). Listeria Monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Specialty-Farms, LLC voluntarily recalled sprouts on July 23, 2010 after laboratory analysis found positive results from one retail sample.
All products dated 7/27/2010 and beyond are not included in this recall.
The above items were distributed to the following companies:
1. Price Chopper (Retailer)
2. Cooseman’s NY (Distributor)
Products have been distributed in the following states: NY, CT, MA, NH, VT, PA
Specialty-Farms, LLC is currently in the process of determining exactly where this potential Lm contamination could be occurring in its facility and is immediately remedying the potential sources as they are identified. Specialty Farms, LLC hopes to return to full sprout production soon.
Consumers who have purchased this product are urged to return them to the point of purchase for refund and may contact Specialty-Farms, LLC with questions at (203) 366-6919 between the hours of 9:00 A.M. to 5:00 P.M. EST.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Pasco Processing LLC, Announces Voluntary Product Recall Because of Possible Health Risk
Contact:
1-800-575-8909
FOR IMMEDIATE RELEASE -- July 21, 2010 - Pasco Processing, LLC, Pasco WA is recalling 2087 cases of 20lb. bulk packaged Corn and Poblano peppers, (SKU 10071179017738) because of the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant women.
No illnesses have been reported in association with the recall. No other products that were manufactured by Pasco Processing, LLC are involved in this recall. This item was produced by Pasco Processing, LLC and transferred to the J R Simplot Company for distribution. The product was packaged in 20 lb bulk cases which were labeled as follows:
Corn and Poblano Blend; 10071179 017738; 20 lbs. Net Wt.; Distributed by J. R. Simplot Co., Boise, Idaho 83707
The recall extends only to products coded 3901741007 and 3901751007 sold to two foodservice distributors in California and one in Arizona and further distributed to Chipotle Mexican Grill Restaurant locations in California, Nevada, and Arizona. The recalled product has been removed from the Chipotle locations and quarantined for destruction. None of the production time periods found to contain Listeria monocytogenes were delivered to restaurants.
Pasco Processing, LLC and Chipotle are collaborating closely with the FDA. The recall is being issued out of an abundance of caution based on a confirmed positive result for Listeria monocytogenes in a routine test sample conducted by the company.
For additional details call Pasco Processing LLC @ 1-800-575-8909 M-F 8:00AM – 4:00PM MDT
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Specialty Farms, LLC Expands Recall of Organic Alfalfa Sprouts Blend and Organic Sprout Salad in the North Eastern United States Because of Possible Health Risk
Contact:
Specialty-Farms, LLC
(203) 366-6919
FOR IMMEDIATE RELEASE -- July 29, 2010 - Specialty Farms is voluntarily recalling certain Alfalfa sprout products with a best if sold by date of "8/3/2010" and "8/1/2010" that has the potential to be contaminated with Listeria Monocytogenes (LM). Listeria Monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Lm infection can cause miscarriages and stillbirths among pregnant women.
Specialty-Farms, LLC is voluntarily recalling Specialty Farms brand Organic Alfalfa Sprouts Blend and Organic Sprout Salad, 4 ounces plastic containers, both have a best if sold by date of 8/3/2010 as noted below:
Brand Item Description UPC
Specialty Farms Organic Alfalfa Sprouts Blend 509800108
Specialty Farms Organic Sprout Salad 8192400024
Specialty-Farms, LLC is also voluntarily recalling Stop & Shop brand Natures Promise Organic Alfalfa Sprouts 4 ounce container and 8 ounce bag and Natures Promise Organic Zesty Sprouts 4 ounce, best if sold by date of 8/1/2010, as noted below. [Further identification on the package includes the following: Certified Organic by NOFA-NY, Certified Organic LLC.]
Brand Item Description UPC
Natures Promise Organic Alfalfa Sprouts (4 oz) 8826704741
Natures Promise Organic Alfalfa Sprouts (8 oz) 8826704102
Natures Promise Organic Zesty Sprouts (4 oz) 8826703903
The products have been distributed thru distributors and to retail stores in CT, NH, MA, ME, NJ, NY, PA, RI, VT.
Specialty-Farms, LLC voluntarily recalled sprouts on July 29, 2010 after laboratory analysis found positive results from retail samples. No illnesses have been reported.
All products dated 8/4/2010 and beyond are not included in this recall
Specialty-Farms, LLC is currently in the process of determining exactly where this potential LM contamination could be occurring in its facility and is immediately remedying the potential sources as they are identified. Specialty Farms, LLC hopes to return to full sprout production soon.
Consumers who have purchased this product are urged to return them to the point of purchase for refund and may contact Specialty-Farms, LLC with questions at (203) 366-6919 between the hours of 9:00 A.M. to 5:00 P.M. EST.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Fresh Express Announces Precautionary Recall of a Limited Number of Cases of Veggie Lovers Salad with an Expiration Date of August 10 Due to a Possible Health Risk
Media Contact:
Ed Loyd, (513) 784-8935, or
Barbara Hines, (972) 724-3049
FOR IMMEDIATE RELEASE -- August 10, 2010 Salinas, California – Fresh Express is voluntarily recalling 2,825 cases of Veggie Lovers Salad with a Product Code of I208 and Use-by Date of August 10, 2010 out of an abundance of caution due to a possible health risk from Listeria monocytogenes. No other Fresh Express salads are included in the recall. No illnesses have been reported in association with the recall.
Only the Veggie Lovers salad products with a Product Code of I208 and a Use-by Date of August 10 are included in the recall. Retailers and Consumers who have any remaining product should not consume it, but rather discard it. Retailers and Consumers with questions may call the Fresh Express Consumer Response Center at (800) 242-5472, Monday – Friday, 5 a.m. – 8 p.m., Pacific Time. Consumers can find the Product Code and Use-by Date in the upper right-hand corner of the package.
This precautionary recall is being conducted to reach retailers as well as consumers. Consumers should check their refrigerators for Fresh Express Veggie Lovers salad with a Product Code of I208 and a Use-by Dates of August 10, 2010. If they have the product, they should immediately discard it. Retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Fresh Express customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is not in the stream of commerce. Although limited in number, the cases were distributed by Fresh Express to 13 states with the potential for redistribution by customers to an additional 14 states (see listing).
Listeria monocytogenes is a bacterium that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. If it spreads to the nervous system symptoms may include headache, stiff neck or confusion. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
The precautionary recall notification is being issued due to an isolated instance in which one package of Fresh Express Veggie Lovers Salad yielded a positive result for Listeria monocytogenes in a random sample test collected and conducted by the Ohio Department of Agriculture.
Fresh Express is coordinating closely with regulatory officials. Immediately upon learning about the positive test result, Fresh Express conducted a traceability assessment and a full review of its food safety documentation, all of which were found to be in compliance and were negative for the presence of any bacteria.
States Distributed Possible Redistribution States
MO, MI, OH, IL, WI, IN, MD, MA, NY, KS, KY, PA, NJ AR, TN, WV, IA, MN, DC, VA, VT, NH, NE, RI, PA, CT, MS
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Morningland Dairy Conducting Nationwide Voluntary Recall of All Cheese Labeled as Morningland Dairy & Ozark Hills Farm Because of Possible Health Risk
Company Contact:
Tel: 417-469-3817, Friday 8 a.m.-4 p.m
Fax: 417-469-5086
morningland@centurytel.net
FOR IMMEDIATE RELEASE - August 30, 2010 - Morningland Dairy of Mountain View, Missouri, is recalling 68,957 pounds of cheese because it may be contaminated with Listeria monocytogenes and also has the potential to be contaminated with Staphylococcus aureus.
Morningland Dairy’s raw milk cheese is sold in the lower 48 states via mail order, retail stores, crop sharing associations, and direct delivery. The cheese is packaged in vacuum-sealed plastic packages that are sold as random weight size retail packages. The specific varieties of cheese are sold under the following brand names and flavors:
Morningland Dairy Raw Milk Cheese (from cow milk): Colby, Hot Pepper Colby, Garlic Colby, Italian Colby, Dill Colby, No-Salt Added Mild Cheddar, Mild Cheddar, Medium Sharp Cheddar, Sharp Cheddar.
Ozark Hill Farms Raw Goat Milk Cheese: Colby, Hot Pepper Colby, Italian Colby, Garlic ‘N’ Chive Colby, Mild Cheddar, Medium Sharp Cheddar, Sharp Cheddar.
The codes affected by the recall are handwritten on the front of the label, and range from A10 (representing January 1, 2010) through F250 (representing June 25, 2010).
NO ILLNESSES HAVE BEEN REPORTED TO DATE.
The recall is a result of regulatory sampling in the State of California. This regulatory sampling of Morningland Dairy cheese, which was taken from the Rawesome store in Venice, California, revealed the Morningland Dairy Hot Pepper Colby and Garlic Colby Cheeses contained the bacteria. Morningland Dairy has suspended the production and distribution of all cheese, as FDA, the Missouri Milk Board, and Morningland Dairy continue their investigation as to the root cause of the problem.
Customers who have purchased the cheese should not eat it, and customers are asked to contact us for instructions, by contacting us at (417) 469-3817 Monday through Friday 8 a.m.-4 p.m., FAX (417) 469-5086, or by e-mailing us at morningland@centurytel.net. Customers can also check our web site for updates over the next several days: www.morninglanddairy.com9.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
QUESERIA CHIPILO INC. Recalls Cheese Products Because of Possible Health Risk
Company Contact:
61 Willet St
Passaic NJ, 07055
(973)-685-7148; (301)-433-1098
For Immediate Release – August 26, 2010 QUESERIA CHIPILO INC. is announcing a recall of the following cheese products, all date codes up to and including September 26, 2010 – Fresco and Nov 25, 2010 – Oaxaca.
Oaxaca String Cheese
Queso Fresco
The Cheese products may be contaminated with Listeria monocytogenes. This is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms, such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, infection can cause miscarriages and still births among pregnant women.
The recalled cheese was distributed in New Jersey, New York, Maryland, Delaware, CT, and Virginia to retail stores and wholesalers.
THE PRODUCT IS SOLD UNDER THE BRAND NAMES OF
QUESERIA CHIPILO
CHIPILO
AZTLAN
For chart of UPC codes go here: http://www.fda.gov/Safety/Recalls/ucm224627.htm
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Sprouts seem to be a problem. And bagged salads.
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Recall -- State Press Release
FDA posts press releases and other notices of recalls and safety alerts from states as a service to consumers, the media, and other interested parties. FDA is not responsible for the content of these notices.
DSHS Orders Sangar Produce to Close, Recall Products
News Media Contact:
Carrie Williams, Press Officer,
512-458-7119 or 512-965-7198
FOR IMMEDIATE RELEASE - October 20, 2010 - The Texas Department of State Health Services today ordered Sangar Fresh Cut Produce in San Antonio to stop processing food and recall all products shipped from the plant since January. The order was issued after laboratory tests of chopped celery from the plant indicated the presence of Listeria monocytogenes, a bacterium that can cause severe illness.
State law allows DSHS to issue such orders when conditions exist that pose "an immediate and serious threat to human life or health."
The recalled products – primarily cut fresh produce in sealed packages – were distributed to restaurants and institutional entities, such as hospitals and schools, and are not believed to be sold in grocery stores.
The testing was done as part of a DSHS investigation into 10 listeriosis cases, including five deaths, reported to the department over an eight-month period. Six of the 10 cases have been linked to chopped celery from the Sangar plant. The illnesses occurred in Bexar, Travis and Hidalgo counties. All of the illnesses were in people with serious underlying health problems.
Health officials said pinpointing a Listeria source is often difficult due to the small number of cases, the illness' long incubation period and difficulty collecting complete information about what people ate.
DSHS inspectors also found sanitation issues at the plant and believe the Listeria found in the chopped celery may have contaminated other food produced there. The department found a condensation leak above a food product area, soil on a preparation table and hand washing issues. DSHS food safety personnel are contacting distributors, restaurants and institutions believed to have received the recalled products to ensure they are taking appropriate action to protect consumers.
DSHS continues to investigate possible sources of contamination and where the products were distributed. Sangar's customers are advised to discard or return the products. Cooking the products is not recommended.
Symptoms of listeriosis can include fever, muscle aches, diarrhea and vomiting. People with these symptoms should consult a physician. Symptoms typically occur three to 70 days after exposure. The disease affects primarily older people, pregnant women, newborns and people with weakened immune systems.
The order prohibits the plant from reopening without DSHS approval.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Bravo Farms announces cheese recall, some products sold under Whole Foods Market label in 5 Western states
Company Contact:
Libba Letton, Whole Foods Market media contact
libba.letton@wholefoods.com
Whole Foods Market
512-542-0878
FOR IMMEDIATE RELEASE - AUSTIN, TX (November 24, 2010) - Whole Foods Market announces that one of its suppliers, Bravo Farms of Traver, California, has issued a voluntary recall due to evidence of Listeria and E. coli contamination at their plant. Bravo’s products at Whole Foods Market stores in Arizona, California, Nevada, Oregon, and Washington are part of this recall since they were cut and packaged in clear plastic wrap and sold with a “Distributed by Whole Foods Market” sticker.
All of the following products are included in this recall:
* Sage Cheddar
* Silver Mountain Cheddar
* Chipotle Cheddar
* Premium Block Cheddar
* Premium White Chunk Cheddar
* Chipotle Chunk Cheddar
* White Black Wax Cheddar
Signage is posted in Whole Foods Market stores to notify customers of this recall.
No illnesses have been reported to date.
Consumers who have purchased any of the listed products from Whole Foods Market may return them to the store for a full refund.
Consumers with questions may contact Whole Foods Market at 512-542-0878.
E. coli O157:H7 causes diarrhea illness often with bloody stools. Although most healthy adults can recover completely within a week, some people can develop a form of kidney failure. Young children and the elderly are most susceptible to serious complications and even death. Listeria can cause listeriosis among at risk people, including pregnant women, newborns, older adults, and people with weakened immune systems. Symptoms include fever, muscle aches, and sometimes nausea or diarrhea. If infection spreads to the nervous system, symptoms such as headache and stiff neck can occur. Infected pregnant women may experience only a mild, flu like illness; however, infections during pregnancy can lead to more serious problems for the fetus. Consumers should seek immediate medical care if they develop these symptoms.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Surtex Foods Recalls “Oaxaca String Cheese La Original” Because Of Possible Health Risk
Contact:
Surtext Foods Co.
323-357-5900
FOR IMMEDIATE RELEASE - January 10, 2011 - SURTEX FOODS CO. of Los Angeles is recalling Oaxaca string Cheese La Original in their 17.63 oz/ 500 gr presentation because it has the potential to be contaminated with Listeria monocytogenes and Staphylococcus aureus.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Staphylococcus aureus the bacterium responsible for producing toxins in foods, can cause gastrointestinal illness that usually begins 1-6 hours after eating contaminated food. The most common symptoms include nausea, vomiting, stomach cramps, and diarrhea. In more severe cases, headache, muscle cramping, and temporary changes in blood pressure and pulse rate may occur. The illness is usually mild and most patients recover after one to three days. In a small minority of patients the illness may be more severe. In these cases, some people, especially the very young and old, may require medical treatment for dehydration from vomiting and/or diarrhea.
Oaxaca String Cheese “La Original” ( 17.63 /500 gr presentation) was distributed in California through retail stores and distributors.
The recalled product comes in a 17.63 ounce (500 gr), clear plastic package marked- Oaxaca String Cheese, “La Original de Oaxaca” with a UPC code of 8 90512 00104 2, Lot # 1360912 with expiration date 01/09/2011
No illnesses have been reported to date.
The recall was the result of a routine sampling program by the FDA which revealed that the finished products contained the bacteria. The company has ceased the production and distribution of the product as FDA and the company continue their investigation as to what caused the problem. NO OTHER PRODUCTS OR BATCHES FROM THIS COMPANY AND/OR PRODUCT THAT HAVE BEEN DISTRIBUTED WERE AFFECTED BY THIS RECALL.
Consumers who have purchased “Oaxaca String Cheese “La Original” ( 17.63 /500 gr presentation), UPC code of 8 90512 00104 2, Lot # 1360912 with expiration date 01/09/2011, are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at (323) 357-5900 Monday through Friday, 8am through 3pm PST.
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* 8-ounce boxes of Ian’s Wheat Free, Gluten Free Mac and No Cheese with a use-by date of 26Aug2011 and UPC code 7-49512-43670-8 (372 packages impacted)
* 8-ounce boxes of Ian’s Wheat Free, Gluten Free French Bread Pizza with a use-by date of 28Aug2011 and UPC code 7-49512-91572-2 (120 packages impacted)
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Ian's Voluntarily Recalls Two Products Due To Risk Of Contamination By Listeria Bacteria
Media Contact:
Laura Kuykendall
1-800-543-6637
media@iansnaturalfoods.com
Consumer Contact:
1-800-543-6637
customerservice@iansnaturalfoods.com
FOR IMMEDIATE RELEASE - January 24, 2011 - Ian’s is voluntarily recalling specific lot numbers of two products due to a risk of contamination with Listeria monocytogenes. Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy persons may suffer only short-term symptoms such as high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths in pregnant women.
The following two products with the specific use-by dates and UPC codes listed are being recalled because they may have been distributed to retailers nationwide and sold in the frozen foods section of the supermarket:
* 8-ounce boxes of Ian’s Wheat Free, Gluten Free Mac and No Cheese with a use-by date of 26Aug2011 and UPC code 7-49512-43670-8 (372 packages impacted)
* 8-ounce boxes of Ian’s Wheat Free, Gluten Free French Bread Pizza with a use-by date of 28Aug2011 and UPC code 7-49512-91572-2 (120 packages impacted)
A total of 492 individual boxes are potentially affected.
Consumers who purchased the above products with the specific use-by dates and UPC codes listed are asked to return the products to the place of purchase to receive a full refund. Products that do not contain the specific use-by dates and UPC codes listed are not affected by the recall, and can be used by consumers.
Consumers with questions can contact Ian’s at 1-800-543-6637 twenty-four hours a day, seven days a week, or at customerservice@iansnaturalfoods.com.
More information is available on the Ian’s website at www.iansnaturalfoods.com9.
About Ian’s
Ian’s offers an extensive line of great-tasting, better-for-you foods for families on-the-go. Ian’s creates and manufactures frozen entrees, fries, kids meals, breakfast foods, snacks and breadcrumbs. Ian’s also offers several food items designed with special dietary needs in mind. Today, Ian’s is based in Lawrence, Massachusetts and is a certified carbon neutral company through the Canadian GHG Challenge Registry. Products are available nationwide at your local natural and organic retailer, and at the company’s Web site, www.iansnaturalfoods.com10.
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Open this link to see the long list of recalls: http://www.fda.gov/Safety/Recalls/ucm241088.htm
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
State Garden, Inc. Announces Voluntary Recall Of Certain Salad Mixes Due To
Possible Health Risk
Press Contact:
Carin Wamer/Christen Graham
Warner Communications
888-841-6191
Consumer Contact:
888-841-6191
FOR IMMEDIATE RELEASE - January 25, 2010 - State Garden, Chelsea, MA - is conducting a voluntary recall of all Salad products produced in our plant on January 4, 2011 which correspond to trace back codes 45693 and 45703 due to a risk of contamination with Listeria monocytogenes. Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy persons may suffer only short-term symptoms such as high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea, Listeria infections can cause miscarriages and stillbirths in pregnant women.
Please know that NO Listeria illnesses have been linked to any State Garden product.
Salad Products and Blends under this recall were distributed to retail stores on the East Coast under various sizes and packaged under the brand names: Gold Quality, Hannaford, Natures Place, Natures Promise, Roche Bros, Northeast Fresh, Noreast Fresh, Olivia’s Organics, Signature, Wegmans. See attached list for the specific salad product, size, package type and UPC codes.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
PIERRE FOODS Voluntarily Recalls 320 Cases Of PierreTM pb jamwich, LOT 0068035 From Giant-Carlisle Stores IN MD, PA, VA AND WV
Contact:
Mary Patrick
312-573-5470
312-961-9159
FOR IMMEDIATE RELEASE - Mar 11, 2011 - Pierre Foods is voluntarily recalling one lot, 320 cases of PierreTM pb jamwich, crustless peanut butter and strawberry jam sandwiches, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The sandwiches were distributed to Giant-Carlisle stores in Maryland, Pennsylvania, Virginia and West Virginia.
The PierreTM pb jamwich comes in a 12-count red carton and is sold in the freezer section of the grocery store. The product in question is stamped “Best if purchased by 03-11-2011” in the lower right hand corner. The UPC code is 7599921368.
This recall is being conducted out of an abundance of caution after Listeria monocytogenes was detected in one product sample. After discussions with the FDA, Pierre Foods elected to recall the product to ensure consumer safety. There have been no reported illnesses or consumer complaints.
Any consumer with the “Best if purchased by 03-11-2011” product in their freezer can return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-982-7091 from 8:00am – 5:00pm EST.
The plant where the product was manufactured has operated for 19 years with no food safety recalls or other serious problems.
###
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Still eating fish?
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
The Smokehouse LLC Recalls One Batch Of Portier Fine Foods Norwegian Smoked Salmon Because Of Possible Health Risk
Contact:
The Smokehouse
1-914-630-4788
FOR IMMEDIATE RELEASE - March 29, 2011 -The Smokehouse LLC of Mamaroneck, New York, is conducting a voluntary recall of PORTIER FINE FOODS Norwegian Smoked Salmon of various size packages including 4 oz., 8 oz., 16 oz. and random weight sizes, Batch Code 066 only, due to potential contamination with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
PORTIER FINE FOODS Norwegian Smoked Salmon with code 066 was distributed and sold on March 7, 2011 to retailers in NY, NJ, CT.
Batch Code 066 (represents Julian date of March 7, 2011) is located on a white label on the rear of gold boards, which are in clear, vacuum packed packages. This is the only batch code affected. The product was also labeled with an “EXPIRES ON” date of 3/21 (3/21/11). Since the product may be stored frozen, the likelihood exists that the affected code (066) may still be available in consumers’ homes.
Please note that NO Listeria illnesses have been linked to any product produced by The Smokehouse LLC.
The recall was the result of a routine sampling by the US Food & Drug Administration (FDA). The company has ceased production and distribution of the product as both the FDA and the company continue their investigation as to what caused the problem. We are taking this action as a precautionary measure and are working with the FDA.
Consumers who have purchased PORTIER FINE FOODS Norwegian Smoked Salmon with code 066 should not consume it and should return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-914-630-4788 Monday through Friday from 9:00 am to 5:00 pm EDT.
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Still eating fish?
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Woodsmoke Provisions Voluntarily Recalls 160 packages of 4 oz. The Fresh Market Signature Collection Atlantic Smoked Salmon Due to Possible Health Risk
Contact:
404-355-5125
FOR IMMEDIATE RELEASE - April 18, 2011 – Woodsmoke Provisions, LLC is voluntarily recalling forty pounds (40 lbs.) / 160 packages of the The Fresh Market Signature Collection Atlantic Smoked Salmon in 4 oz. retail packages with lot code 1459/2, because they have the potential to be contaminated with Listeria monocytogenes.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infections can cause miscarriages and stillbirths among pregnant women.
The 160 packages of product subject to recall were distributed and sold only in a limited number of The Fresh Market, Inc. stores located in AR, FL, GA, IL, KY, MD, NC, OH and TN.
The product being recalled was packaged in 4 oz. plastic packages with the specific lot code 1459/2 which was manufactured January 15, 2010. The item UPC code is 737094000370.
No illnesses have been reported to date.
The potential for contamination was noted after routine inspection by the Florida Department of Agriculture and Consumer Services.
Consumers who have purchased this product from one of the above-mentioned stores with lot code 1459/2 should not consume it, and are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 404-355-5125, Monday through Friday from 9am to 5pm (EST).
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Goodness Gardens, Inc. Recalls Chives Lot # 0201111 Because of Possible Health Risk
Contact:
Consumer:
845-355-4757
FOR IMMEDIATE RELEASE - May 10, 2011 - Goodness Gardens, Inc. of New Hampton, NY is voluntarily recalling Chives Lot # 0201111, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The Chives were distributed in NY, NJ, CT, MA, PA, MD, AL, IL, and VA through retail stores primarily
and one wholesaler in PA.
The Chives were distributed in various plastic clamshell containers: 0.25 oz. (UPC 0 21985 20005 6), 2/3 oz.
(UPC 0 21985 10004 2), in 1 lb. bags, and ½ oz. twist tie bunches.
No other Goodness Gardens Inc. products or lots are included in this recall.
The recall was the result of a routine sampling program by the Connecticut Department of Consumer Protection which revealed that the product lot contained the bacteria.
It is unlikely that any product still remains in stores but if so retailers should remove Chives Lot # 0201111 with date 5/6/11 from store shelves and inventories. Goodness Gardens, Inc. Customer Service representatives are already contacting retailers to ensure the precautionary recall is executed swiftly.
The company is not aware of any illnesses reported in connection with the recall and is coordinating
closely with regulatory officials.
Consumers are urged not to consume the above lot. Consumers who purchased this item are urged to return it to the place of purchase for a full refund. Consumers with questions can contact Goodness Gardens, Inc. at 845-355-4757, Mon – Fri 9am - 4pm EDT with any questions.
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Nielsen-Massey Vanillas, Inc. Issues Voluntary Recall for Specific Lot of Madagascar Bourbon Pure Vanilla Bean Paste
Tue, 17 May 2011 17:15:00 -0500
Nielsen-Massey Vanillas, Inc. of Waukegan, Illinois is voluntarily recalling lot no. 11123 of its Nielsen-Massey Madagascar Bourbon Pure Vanilla Bean Paste because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
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Schratter Foods Inc RECALLS "Quenby Hall Blue Stilton Cheese" BECAUSE OF POSSIBLE HEALTH RISK
Wed, 18 May 2011 15:15:00 -0500
“Quenby Hall Blue Stilton Cheese” is being recalled by Schratter Foods Incorporated, a Fairfield, New Jersey-based food distributor, because the product has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
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(http://i587.photobucket.com/albums/ss316/TROPhotobucket/ucm260505.jpg)
(http://i587.photobucket.com/albums/ss316/TROPhotobucket/ucm260507.jpg)
(http://i587.photobucket.com/albums/ss316/TROPhotobucket/ucm260508.jpg)
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Italian Blend Salads
Contact:
Consumer:
(800) 356-3111
Media:
Marty Ordman
(818) 874-4834
marty.ordman@dole.com
FOR IMMEDIATE RELEASE - June 22, 2011 - Dole Fresh Vegetables is voluntarily recalling 2,880 cases of DOLE® Italian Blend salad with Use-by Date of June 19, 2011, UPC code 7143000819 and Product Codes 0049A157201A, 0049A157201B, 0049A157202A, 0049A157202B, 0686A157202A, 0686A157202B and 442 cases of Kroger Fresh Selections Italian Style Blend salad with Use-by-Date of June 19, 2011, UPC code 1111091045 and Product Codes A157201A & A157201B, due to a possible health risk from Listeria monocytogenes. Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported in association with the recall.
The Product Code and Use-by Date are in the upper right-hand corner of the package; the UPC code is on the back of the package, below the barcode. The salads were distributed in twelve U.S. states (Illinois, Indiana, Kentucky, Maine, Michigan, Mississippi, New Jersey, New York, Ohio, Pennsylvania, Tennessee and Wisconsin) and three Canadian provinces (New Brunswick, Ontario and Quebec).
No illnesses have been reported in association with the recall. This precautionary recall notification is being issued due to an isolated instance in which one package of Dole Italian Blend salad yielded a positive result for Listeria monocytogenes in a random sample test collected and conducted by the Ohio Department of Agriculture.
No other Dole or Kroger salads are included in the recall. Only the specific Product Codes, UPC codes and June 19, 2011 Use-by-Date of Italian Blend salads identified above are included in the recall. Consumers who have any remaining product with these Product Codes should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Food Company Consumer Response Center at (800) 356-3111, which is open 8:00 am to 3:00 pm (PDT) Monday - Friday.
Retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Dole Fresh Vegetables customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is not in the stream of commerce.
Listeria monocytogenes is a bacterium that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. If it spreads to the nervous system symptoms may include headache, stiff neck or confusion. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Fresh & Easy Neighborhood Market Voluntarily Recalls One Date Code Of f&e™ Brand Organic Baby Spinach Because Of Possible Health Risk
Contact:
Consumer:
800-648-8622
Media:
Brendan Wonnacott
310-872-7613
brendan.wonnacott@freshandeasy.com
FOR IMMEDIATE RELEASE - August 5, 2011 - Fresh & Easy Neighborhood Market Inc., is voluntarily recalling fresh Organic Baby Spinach with the Enjoy by date of Aug 01 sold under the f&e™ label.
The recall notification is being issued out of an abundance of caution based on a random sample test, conducted on behalf of the Food & Drug Administration (FDA). One bag of this product with the Aug 01 Enjoy by date was confirmed to be positive for Listeria monocytogenes. No illnesses have been associated with this product.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
Fresh & Easy believes that it is important to alert consumers that might still possess this product with the Enjoy by date of Aug 01. Customers still in possession of this expired product should immediately dispose of it.
Product Description Barcode Dates Affected
f&e™ Organic Baby Spinach
5 oz.(142g) Plastic Bag
20001162 Enjoy by
Aug 01
The recalled product was sold in Fresh & Easy Neighborhood Market stores located in California, Nevada, and Arizona.
Customers may return the empty product bag or present the receipt as proof of purchase of the recalled product to any Fresh & Easy store for a full refund. Consumers who have questions or concerns about this recall should contact the Fresh & Easy 24-hour toll free number at 1 (800) 648-8622.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
FRESH FOOD CONCEPTS, INC. RECALLS LAYER DIP PRODUCTS CONTAINING GUACAMOLE BECAUSE OF POSSIBLE HEALTH RISK
Contact:
Consumer Contact:
714-562-5000 ext. 134
Media Contact:
Dale Jabour
FOR IMMEDIATE RELEASE - August 12, 2011 - Fresh Food Concepts, Inc. of Buena Park, CA is voluntarily recalling various Layer Dip products containing guacamole because the avocado has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The product was distributed nationwide and Canada through retail supermarkets and club stores.
The product can be identified as follows:
Product Description UPC Code Use By date code
Fresh Food Concepts 5 Layer Dip, 32 oz 29358-11272 09/16/11 and before
Delicioso 5 Layer Dip, 15 oz 29358-12229 09/16/11 and before
Delicioso 5 Layer Dip, 30 oz 29358-12230 09/16/11 and before
Rojo’s Ultimate 7 Layer Dip, 36 oz 35196-44162 09/16/11 and before
Fresh Food Concepts 5 Layer Dip, 16 oz 35196-44216 09/16/11 and before
Rojo’s Supreme 6 Layer Dip, 44 oz 47502-44180 09/16/11 and before
Rojo’s 6 Layer Dip, 44 oz 47502-44185 09/16/11 and before
Rojo’s 6 Layer Dip, 44 oz 47502-44189 09/16/11 and before
Fresh Food Concepts 5 Layer Dip, 454 g 35196-44214 09/16/11 and before
Signature Café 6 Layer Dip, 15 oz 21130-06191 09/16/11 and before
Signature Café 6 Layer Dip, 30 oz 21130-06192 09/16/11 and before
Signature Café 6 Layer Dip, 425 g 58200-06034 09/16/11 and before
Signature Café 6 Layer Dip, 850 g 58200-06032 09/16/11 and before
Product with expiration dates USE BY 09/24/11 and AFTER are made with avocado from a different source and are NOT involved in this recall. No other products made by Fresh Food Concepts are involved in this recall.
This recall was the result of a routine sampling program by the FDA which revealed that the imported AVOCADO PULP used in these products contained the bacteria. The company has ceased the use of avocado from the supplier.
Consumers who have purchased the recalled product are urged to return it to the place of purchase for a full refund or destroy it. Consumers with questions may contact the company at 1-714-562-5000 ext 134, Monday – Friday, 8:00 AM – 5:00 PM PDT.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Atlanta Oriental Food Recalls Cut Napa Kimchi Because Of Possible
Listeria Monocytogenes
Contact:
Consumer:
Tristan Thompson
404-379-3333
FOR IMMEDIATE RELEASE - August 17, 2011 - Atlanta Oriental Food Wholesale Company of Atlanta, GA, is recalling its 1 gallon plastic containers of Cut Napa Kimchi and 5 gallon buckets of Cut Napa Kimchi because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled Kimchi was distributed at Buford Highway Farmers Market in Doraville, Georgia as well as in five gallon buckets to companies in Georgia, Alabama and Tennessee.
The product comes in a 1 gallon, clear plastic package and a 5 gallon bucket marked with lot # 56090959 on the side of the containers.
The potential for contamination was noted after routine testing by the company revealed the presence of Listeria monocytogenes in 1 gallon containers of Cut Napa Kimchi.
The production of the product has been suspended while FDA and the company continue to investigate the source of the problem.
Consumers who have purchased 1 gallon containers and 5 gallon buckets of Cut Napa Kimchi with lot # 56090959 are urged to return them to the place of purchase for a full refund. Consumers with questions may contact Tristan Thompson, Monday thru Friday from 10 am to 6 pm at 404-379-3333.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Fine Mexican Food Products, Inc. Recalls 2.2 lb. Frozen Avocado Pulp & 3 lb. IQF Avocado Halves From Peru Because of Possible Health Risk
Contact:
Consumer
909 947-4296
FOR IMMEDIATE RELEASE - September 13, 2011 - Fine Mexican Food Products, Inc. (FMP) located in the City of Ontario in California is recalling 1,423 Cases of 12/2 lb. Frozen Avocado Pulp and 1,820 Cases IQF 8/3 lb. IQF Avocado Halves as distributed since June/2010 because of the possibility to be contaminated with Listeria Monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Frozen avocado pulp and IQF avocado halves were distributed to distributors in California since June 2010.
These 2 products are identified as FMP white label on the corrugated shipping carton and pack size is 2.2 lb. /bag 12 per shipping carton and Product code 00115 for Frozen Avocado Pulp.
Pack size is 3 lb. /bag 8 bags per shipping carton and Product Code 00131 for 3 lb. IQF Avocado Halves respectively with expiration dates of June/July/August 2012.
We have not received any report of illness related to the products.
The recall was the result of multiple positive Listeria Monocytogenes results in 20 lbs. size avocado pulp manufactured at the same facility in Peru. FMP is recalling out of an abundance of caution. FMP is a responsible company and cares about protecting the public health. If you have these products in your position, please return the product to distributors as soon as possible. FMP has ceased the production, importing and distribution of the product as FDA and the company continues their investigation as to what caused the problem."
For more information please call to Fine Mexican Food Products, Recalls Procedures at 909 947-4296.
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NM Issues Voluntary Cantaloupe Recall Notice; Multistate Listeriosis Outbreak Update
CDC issues cantaloupe warning after Listeria outbreak
Tuesday, September 13, 2011 at 7:03 pm
NM Issues Voluntary Cantaloupe Recall Notice; Multistate Listeriosis Outbreak Update
The New Mexico Environment Department’s (NMED) Environmental Health Bureau, in conjunction with the New Mexico Department of Health (DOH) is issuing a voluntary recall notice all state produce retailers, requesting that any cantaloupe grown in the Rocky Ford growing area of southern Colorado be temporarily pulled from store shelves. The Bureau is announcing this voluntary recall in anticipation of a nationwide recall in the near future. Likewise, early indications from several states, including New Mexico, link the recent Listeriosis outbreak to these cantaloupes.
The New Mexico Department of Health (DOH)has identified ten cases of Listeria infection to date, with three of these cases resulting in death. In New Mexico, all 9 patients who have been interviewed reported eating cantaloupe prior to illness.
All of the ill people in New Mexico have been hospitalized, including the three fatalities.The fatal cases were: a 93-year-old man from Bernalillo County, a 61-year-old female from Curry County, and a 63-year-old man from Bernalillo County. The other hospitalized cases in New Mexico come from Bernalillo, Chaves, Otero, De Baca, Valencia and Lea counties. The ill people range in age from the 43 to 96 and include 4 men and 6 women. Illness onset ranges from August 20 to early September.
Source (http://www.lamonitor.com/content/nm-issues-voluntary-cantaloupe-recall-notice-multistate-listeriosis-outbreak-update)
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FDA Warns Consumers About Potentially Contaminated Cheese
Mon, 09 Mar 2009 17:24:00 -0500
The U.S. Food and Drug Administration is warning consumers not to eat Queso Fresco Fresh Cheese Mexican style soft cheese (two specific lots) or any Queso Cotija Molido Mexican style grated cheese manufactured and distributed by Peregrina Cheese Corp. of New York City. These products could be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in pregnant women, young children, frail or elderly people, and others with weakened immune systems.
Another recall of this type cheese:
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Del Bueno Recalls Queso Fresco Casero Cheese Because of Possible
Health Risk
Contact:
Consumer:
Jesus Rodriguez
425-503-3823
FOR IMMEDIATE RELEASE - September 16, 2010 - Del Bueno of Grandview, WA is recalling all 16oz. size packages of Queso Fresco Casero Fresh Cheese with a date stamp of Sept 14, 2011 because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Queso Fresco Casero Fresh Cheese was sold in retail markets in Washington and at the Pasco, WA flea market.
The cheese is packaged in round clear plastic 16oz. packages, and is stamped on the back with a code date of “Sep 14 2011”.
This recall is the result of a routine sampling program by Washington State Department of Agriculture which revealed that the cheese is contaminated with Listeria. The company will be notifying their customers and requesting that they stop sales of this product. Del Bueno is working with FDA to conduct their recall.
Consumers who have purchased Del Bueno brand Queso Fresco are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 425-503-3823 between 8:00am and 4:00pm Pacific time.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Publix Recalls Spinach Dip Due To Possible Health Risk
Contact:
Consumer:
1-800-242-1227
www.publix.com
Media:
Maria Brous
863-680-5339
FOR IMMEDIATE RELEASE - September 26, 2011 - Publix Super Markets is issuing a voluntary recall for spinach dip because it may be adulterated with Listeria monocytogenes. The problem was discovered as a result of routine microbial testing conducted by Publix. The 16 ounce containers of prepackaged spinach dip were sold at Publix retail deli departments with a UPC of 41415-00062 and use by date of OCT 10 C1.
Consumption of products containing Listeria monocytogenes can cause serious and sometimes fatal infection in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
No illnesses have been reported to date in connection with this problem.
The spinach dip was sold in Publix grocery stores in Florida. The following counties in Florida did not receive recalled product: Miami-Dade, Broward, Palm Beach, Martin, St. Lucie, Indian River, and Okeechobee. Publix stores in Alabama, Georgia, South Carolina, and Tennessee are not involved with this recall.
"As part of our commitment to food safety, potentially impacted product has been removed from all store shelves,” said Maria Brous, Publix media and community relations director. "To date, there have been no reported cases of illness. Consumers who have purchased the products in question may return the product to their local store for a full refund. Publix customers with additional questions may call our Consumer Relations department at 1-800-242-1227 or by visiting our website at www.publix.com." Customers can also contact the US Food and Drug Administration at 1-888-SAFEFOOD (1-888-723-3366).
Publix is privately owned and operated by its 147,500 employees, with 2010 sales of $25.1 billion. Currently Publix has 1,038 stores in Florida, Georgia, South Carolina, Alabama and Tennessee. The company has been named one of Fortune's "100 Best Companies to Work For in America" for 14 consecutive years. In addition, Publix’s dedication to superior quality and customer service is recognized as tops in the grocery business, most recently by an American Customer Satisfaction Index survey.
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NM Issues Voluntary Cantaloupe Recall Notice; Multistate Listeriosis Outbreak Update
CDC issues cantaloupe warning after Listeria outbreak
Tuesday, September 13, 2011 at 7:03 pm
NM Issues Voluntary Cantaloupe Recall Notice; Multistate Listeriosis Outbreak Update
The New Mexico Environment Department’s (NMED) Environmental Health Bureau, in conjunction with the New Mexico Department of Health (DOH) is issuing a voluntary recall notice all state produce retailers, requesting that any cantaloupe grown in the Rocky Ford growing area of southern Colorado be temporarily pulled from store shelves. The Bureau is announcing this voluntary recall in anticipation of a nationwide recall in the near future. Likewise, early indications from several states, including New Mexico, link the recent Listeriosis outbreak to these cantaloupes.
The New Mexico Department of Health (DOH)has identified ten cases of Listeria infection to date, with three of these cases resulting in death. In New Mexico, all 9 patients who have been interviewed reported eating cantaloupe prior to illness.
All of the ill people in New Mexico have been hospitalized, including the three fatalities.The fatal cases were: a 93-year-old man from Bernalillo County, a 61-year-old female from Curry County, and a 63-year-old man from Bernalillo County. The other hospitalized cases in New Mexico come from Bernalillo, Chaves, Otero, De Baca, Valencia and Lea counties. The ill people range in age from the 43 to 96 and include 4 men and 6 women. Illness onset ranges from August 20 to early September.
Source (http://www.lamonitor.com/content/nm-issues-voluntary-cantaloupe-recall-notice-multistate-listeriosis-outbreak-update)
CNN video: http://www.cnn.com/video/?hpt=he_mid#/video/health/2011/09/28/sosa-tainted-cantaloupe.cnn
From the time one ingests listeria bacteria, it may take up to 70 days to become ill.
(CNN) -- Federal health officials are expanding efforts to ensure no additional bacteria-tainted cantaloupes get to consumers in what has become the deadliest U.S. outbreak of a food-borne illness in more than a decade.
The Food and Drug Administration said it has teamed up with state officials in the effort.
"FDA and its state partners are conducting checks at retail stores, wholesalers and distributors to make sure they have received notification about the Jensen Farms' whole cantaloupe recall and that they have taken appropriate action to notify their customers and remove the recalled whole cantaloupes from the shelves," the agency said in a statement Wednesday.
As of Monday, it had grown to 18 states, 72 illnesses and 13 deaths, according to the CDC's latest statistics.
What you need to know about Listeria monocytogenes (http://thechart.blogs.cnn.com/2011/09/28/faqs-of-listeria-monocytogenes/)
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Jensen Farms Includes IN, LA, and WI in Cantaloupe Recall Notification
Contact:
Consumer:
recall@rfordcantaloupe.com
1-800-267-4561
Media:
Amy Philpott
aphilpott@watsonmulhern.com
FOR IMMEDIATE RELEASE - September 29, 2011 - Jensen Farms of Holly, CO is including whole cantaloupes shipped to the states of Indiana, Louisiana and Wisconsin in its September 14th recall notification.
As part of its ongoing internal review of shipment records, Jensen Farms has identified shipments to these three states as part of the September 14 recall. The whole cantaloupes sent to IN, LA and WI were included in the original volume recalled on September 14, and the customers that received this product from Jensen Farms were notified of the recall on the same day.
“The company has confirmed that its customers, including those who requested that the product be shipped to Indiana, Louisiana or Wisconsin, received the September 14 recall notice to remove the product from commerce immediately,” said Amy Philpott, spokeswoman for Jensen Farms.
Consumers with questions may contact Jensen Farms via email at recall@rfordcantaloupe.com or phone 1-800-267-4561 Monday thru Friday between the hours of 9am and 4pm MST.
The September 14 press release can be found at www.rfordcantaloupe.com.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Note: This recall is not related to the recall of cantaloupe due to Listeria by Jensen Farms of Colorado. No illnesses related to this finding have been reported. The finding of Listeria in romaine lettuce was a result of an FDA research program to understand the prevalence of Listeria in fresh produce, particularly lettuce and leafy greens. FDA will monitor the recall and work with the company to determine the source of the contamination.
True Leaf Farms Announces
Voluntary Recall of Bagged, Chopped Romaine
Contact:
Consumer:
True Leaf Farms
800-799-9475
Media:
Steve Church
831-760-6208
steve@churchbrothers.com
FOR IMMEDIATE RELEASE - September 29, 2011 - True Leaf Farms is voluntarily recalling 90 cartons of chopped romaine because of the potential of contamination with Listeria monocytogenes. The recalled product was shipped between September 12 and 13 to an institutional food service distributor in Oregon who further distributed it to at least two additional states, Washington and Idaho. The romaine affected by this recall has a “use by date” of 9/29/11.
No illnesses related to this finding have been reported
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled bags of romaine were packed in True Leaf Farms cardboard cartons and distributed by Church Brothers, LLC, and shipped between September 12 and 13, 2011. All bags carry a “use by date” of 9/29/11. Produce affected by the recall was labeled as follows:
2# bags, chopped romaine - Bag and box code B256-46438-8
Photos of the recalled product can be viewed at www.churchbrothers.com/recall. This recall includes only chopped romaine as described above.
FDA notified the company today that a sample taken as part of a random check from a single bag of chopped romaine tested positive for Listeria monocytogenes. True Leaf Farms is working with FDA to inform consumers of this recall. In addition, the company is working with its food service distribution customers to ensure that other romaine products that may be implicated are pulled from the market.
“We are fully cooperating with the FDA, and we are contacting all of our customers to ensure prompt removal of any product potentially associated with the recall,” said Steve Church, True Leaf Farms. “We are committed to conducting this recall quickly and efficiently to reduce any risk to public health.”
Anyone who has in their possession the recalled romaine as described above should not consume it, and should either destroy it or call Church Brothers, LLC for product pickup.
Consumers with questions or who need information may call Church Brothers, LLC, the sales agent for True Leaf Farms, at 1-800-799-9475, or may visit www.churchbrothers.com for updates.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Media Statement on Voluntarily Recall of Giant Eagle Farmer's Market Shredded Iceberg Lettuce
Contact:
Consumer:
Dan Donovan
(412) 963-5072
Daniel. Donovan@gianteagle.com
FOR IMMEDIATE RELEASE -October 12 , 2011 -Pittsburgh -Giant Eagle has been informed by representatives of the Food and Drug Administration (FDA) of the presence of listeria monocytogenes in a routine random sample test of Giant Eagle Farmer's Market eight ounce package of Shredded Iceberg Lettuce, produced by River Ranch Fresh Foods LLC, with a use by date of October 14,2011 (see attached product image). To date, there are no reported cases of customer illness due to consumption of this item.
The packaged product affected is Giant Eagle Farmer's Market Shredded Iceberg Lettuce (UPC 3003430195). Additionally, the shredded iceberg lettuce was used in a small number of prepared deli ring sandwiches. The affected deli ring sandwiches include: Giant Eagle Large Italian Sandwich Ring (UPC 23755100000), Giant Eagle Mini Italian Sandwich Ring (UPC 24755500000), Giant Eagle Large New York Sandwich Ring (UPC 22755100000), Giant Eagle Mini New York Sandwich Ring (UPC 25755500000), Giant Eagle Large All America Sandwich Ring (UPC 21755100000), and Giant Eagle Mini All American Sandwich Ring (UPC 26755500000).
Upon receiving the test results from the FDA, Giant Eagle immediately performed a voluntary recall of all potentially affected shredded iceberg lettuce. Giant Eagle implemented a register sale block to ensure that none of the product involved was inadvertently purchased. Giant Eagle also has removed all potentially affected products from its store shelves. Additionally, the company initiated a proactive telephone call to customers who purchased the products with instructions to dispose of the product or return it to the store for a refund (see attached customer call script).
Giant Eagle uses loyalty card purchase history data to contact customers who may be affected by food recalls with a health risk. Giant Eagle Advantage Card holders are encouraged to update contact information in the case of a recent change of mailing address or phone number. To communicate changes in contact information, customers may call 1-800-474-4777.
Finally, according to the Centers for Disease Control (www.cdc.gov), the risk of an individual developing a listeria infection after consumption of a contaminated product is very small. Listeriosis affects primarily persons of advanced age, pregnant women, newborns and adults with weakened immune systems.
Contact:
Dan Donovan
Giant Eagle, Inc.
412.963.5072
Daniel. Donovan@gianteagle.com
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
River Ranch Recalls Products Because of Possible Health Risk
Contact:
Consumer:
Bruce Knobeloch
TEL 831-758-1390
FAX 831-755-8281
FOR IMMEDIATE RELEASE - October 13, 2011 - River Ranch Fresh Foods, LLC of Salinas, CA is initiating a voluntary recall of 2,154 cases of various bagged salad products due to the potential of being contaminated with Listeria monocytogenes following a routine random test conducted by the Ohio Department of Agriculture.
The bagged salad products subject to the recall include:
See list here: http://www.fda.gov/Safety/Recalls/ucm275854.htm
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Fresh & Easy Neighborhood Market Voluntarily Recalls One Date Code Of f&e™ Brand Washed Spinach Because Of Possible Health Risk
Contact:
Consumer:
1 (800) 648-8622
Media:
Brendan Wonnacott
brendan.wonnacott@freshandeasy.com
(310) 384-3833
FOR IMMEDIATE RELEASE - October 21, 2011 - Fresh & Easy Neighborhood Market Inc., is voluntarily recalling fresh bagged Washed Spinach 12oz, with the Enjoy by date of OCT 16 sold under the f&e™ label.
The recall notification is being issued out of an abundance of caution based on a random sample test, conducted on behalf of the Food & Drug Administration (FDA). One bag of this product with the Oct 16 Enjoy by date was confirmed to be positive for Listeria monocytogenes. No illnesses have been associated with this product.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
Fresh & Easy believes that it is important to alert consumers that might still possess this product with the Enjoy by date of Oct 16. Customers still in possession of this expired product should immediately dispose of it.
Product Description
Washed Spinach
12oz.(340g) Plastic Bag
Barcode
20001124
Dates Affected
Enjoy by
OCT 16
The recalled product was sold in Fresh & Easy Neighborhood Market stores located in California, Nevada, and Arizona.
Customers may return the empty product bag or present the receipt as proof of purchase of the recalled product to any Fresh & Easy store for a full refund. Consumers who have questions or concerns about this recall should contact the Fresh & Easy 24-hour toll free number at 1 (800) 648-8622.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Golden Glen Creamery Issues Voluntary Recall of Raw Cheddar Because of Possible Health Risk
Contact:
Consumer
360-766-6455
info@goldenglencreamery.com
FOR IMMEDIATE RELEASE - November 8, 2011 - Golden Glen Creamery of Bow, WA is voluntarily recalling Raw Cheddar because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
To date, no illnesses have been reported.
Approximately twenty (20) pounds of the Raw Cheddar was distributed through a very few, select retail stores in Washington State, as well as at Golden Glen’s on-farm store between September 22 and November 5 of this year. The packages range in size from ¼ to ½ pound pieces, and are random-weight cuts.
The product is vacuum packaged in clear plastic with a stick on label. The label reads in part: “Raw Cheddar,” “GOLDEN GLEN CREAMERY”and“Natural handcrafted cheese produced by the Jensen ladies.” The back of the product has a white sticker with the three-digit code “864.”
The Raw Cheddar is being voluntarily recalled by Golden Glen Creamery, and was a result of a surveillance sample collected and analyzed by the Washington State Department of Agriculture that was found to be positive for Listeria monocytogenes. The company has ceased the production and distribution of the product as FDA, the Washington State Department of Agriculture and the company continues their investigation as to what caused the problem.
Consumers who have purchased the product are urged to destroy the product or return the product to the place of purchase for a full refund. Consumers with questions may contact Golden Glen Creamery at 360-766-6455, from 8:00 AM – 4:00 PM PST, Monday through Friday, or by email at info@goldenglencreamery.com.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Golden Glen Creamery Issues Voluntary Recall Of Butter Because Of Possible Health Risk
Contact:
Consumer:
Golden Glen Creamery
360-766-6455
info@goldenglencreamery.com
FOR IMMEDIATE RELEASE - December 3, 2011 -Golden Glen Creamery of Bow, WA is voluntarily recalling Butter produced on November 2, 2011 because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
To date, no illnesses have been reported.
21 - 4 oz. packages of Herbes de Provence Butter were available at the Whole Foods Market in Redmond, WA. 68 - 4 oz. packages of NW Mushroom Trio Butter were available at the Whole Foods Market in Redmond, WA, and at various Metropolitan Market locations in Washington. Products were distributed between 11/7/11 and 11/28/11 and are in circulation to date.
The product is sold in 4 oz. plastic round containers with tamper-evident seals. The labels read in part: “Herbes de Provence Butter”, or “Northwest Mushroom Trio Butter”, along with “GOLDEN GLEN CREAMERY”and“Natural handcrafted cheese produced by the Jensen ladies.” The top label on the products has a three-digit code “767.”
The Butters are being voluntarily recalled by Golden Glen Creamery, as a result of a surveillance sample collected and analyzed by the Washington State Department of Agriculture that was found to be positive for Listeria monocytogenes. The company has ceased the production and distribution of the product as FDA, the Washington State Department of Agriculture and the company continues their investigation as to what caused the problem.
Consumers who have purchased the product(s) are urged to destroy the product(s) or return the product(s) to the place of purchase for a full refund. Consumers with questions may contact Golden Glen Creamery at 360-766-6455, from 8:00 AM – 4:00 PM PST, Monday through Friday, or by email at info@goldenglencreamery.com.
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Kradjian Imp Co Is Doing An Extended Recall Of Cedar Tree Brand Tresse Cheese And Cedar Tree Brand Shinglish Cheese Because Of Possible Health Risk
01/19/2012 10:07 PM EST
Kradjian Imp Co, Glendale, CA is recalling 231 Cases, 22Lb / Cs of Cedar Tree brand Tresse Cheese, 16 oz and Cedar Tree brand Shinglish cheese, 16 oz because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Alfa Sprouts Inc. (Springwater Sprouts) Recalls Alfalfa Sprouts And Clover Sprouts Due To Possible Health Risk
Contact:
Consumers/Media
585-624-1234
FOR IMMEDIATE RELEASE - April 25, 2012 - Alfa Sprouts Inc. of Honeoye Falls, NY is recalling approx. 100 lbs of Springwater Sprouts brand Organic Alfalfa Sprouts and bulk 3# Clover Sprouts because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections to individuals with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The following 2 products are being recalled by the firm.
Clear clam shell packages containing 4 oz. Organic Alfalfa Sprouts with a sell by date of 4/28/2012. This product was distributed in New York State. Product label and UPC code noted below.
UPC Code 688267047411
UPC Code 042891000523
3# Bulk containers of Clover Sprouts, with a production code of P93. This product was distributed to institutional accounts in Upstate New York.
The contamination was discovered after sampling under the USDA Microbiological Data Program by New York State Department of Agriculture and Markets inspectors and subsequent analysis by the New York State Food Laboratory personnel revealed the presence of Listeria monocytogenes in the product. No illness has been reported to date.
Consumers who have purchased Organic Alfalfa Sprouts or bulk 3 # Clover Sprouts, distributed by Alfa Sprouts Inc. (Springwater Sprouts) should return the product to the place of purchase for a full refund.
Consumers with questions may contact the company at 585 624 1234.
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Recall -- State / Local Press Release
FDA posts press releases and other notices of recalls and safety alerts from states as a service to consumers, the media, and other interested parties. FDA is not responsible for the content of these notices.
Henry’s Farm Inc. Expands Recall Of Soybean Sprouts Due To Possible Health Risk
Contact:
Consumer
301-802-2996 or,
804-786-3520
Media
Mr. Soo Park
301-802-2996
FOR IMMEDIATE RELEASE - April 30, 2012 - Henry’s Farm Inc. is expanding the recall of its Soybean Sprouts, to include Natto Soybean Sprouts, because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections to individuals with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The initial date of the recall was April 27, 2012
The following products are being recalled by the firm.
All clear plastic packages containing 1.5 lbs. Grown in Natural Spring Water Soybean Sprouts. The packages were not coded.
All bulk (approximately 10 lbs.) plastic bags of Soybean Sprouts. The packages were neither coded nor labeled.
All clear plastic packages containing 1 lb. Grown in Natural Spring Water Natto Soybean Sprouts. The packages were not coded.
These items were distributed to retail stores in Virginia, Maryland and Washington D.C.
The contamination was discovered after sampling by VDACS Food Safety and Security Program. Subsequent analysis by the Virginia Division of Consolidated Laboratory Services revealed the presence of Listeria monocytogenes in the products. No illness has been reported to date.
Individuals who purchased Soybean Sprouts distributed by Henry’s Farm should return the product to the place of sale for a full refund.
Consumers with questions may contact either the company directly at 301.802.2996 or the Virginia Department of Agriculture and Consumer Services, Food Safety and Security Program. at 804.786.3520.
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Recall -- State / Local Press Release
FDA posts press releases and other notices of recalls and safety alerts from states as a service to consumers, the media, and other interested parties. FDA is not responsible for the content of these notices.
Cleveland Beansprouts Co. of Cleveland, OH is recalling all alfalfa sprouts because they
may be contaminated with Listeria monocytogenes
CLEVELAND, Ohio (May 4, 2012) - Cleveland Beansprouts Co. of Cleveland, OH is recalling all alfalfa sprouts because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections to individuals with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
All alfalfa sprouts produced by Cleveland Beansprouts are being recalled. There are no lot codes or any other identifier on the product. The alfalfa sprouts were only distributed in Ohio.
The contamination was discovered by the Ohio Department of Agriculture while collecting and testing samples under the United States Department of Agriculture’s Microbiological Data Program. No illnesses have been reported to date.
Consumers who have purchased alfalfa sprouts produced by Cleveland Beansprout should discard them.
Photo: Product Labels
Recalled Product Photos Are Also Available on FDA's Flickr Photostream.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
River Ranch Recalls Retail And Food Service Salads Because Of Possible Health Risk
Contact:
Consumer:
1-800-762-7708
Media:
Kim St George
831-758-1390
FOR IMMEDIATE RELEASE - May 18, 2012 - River Ranch Fresh Foods, LLC of Salinas, CA is initiating a voluntary recall of retail and foodservice bagged salads, because they have the potential of being contaminated with Listeria monocytogenes following routine random retail salad finished product tests conducted in the marketplace by the Food & Drug Administration.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Retail salad products under this recall were distributed nationwide under various sizes and packaged under the brand names of River Ranch, Farm Stand, Hy-Vee, Marketside, Shurfresh, and The Farmer’s Market.
Foodservice salad products under this recall were distributed nationwide under various sizes and packaged under the brand names of River Ranch, Cross Valley, Fresh n Easy, Promark, and Sysco.
The recalled retail and foodservice salad bags have either “Best By” code dates between 12MAY2012 – 22MAY2012 or Julian dates between 116 – 125. The code date is typically located in the upper right hand corner of the bags.
See attached list for the specific salad products, size, package type, UPC codes and states of distribution.
No other products, brands or code dates aside from those listed below are affected by this recall.
There have been NO reported illnesses associated with this recall. We are working closely with the Food & Drug Administration and California Department of Public Health.
Consumers who have purchased this product should not consume it and are urged to return it to the place of purchase for a full refund. Consumers with questions can contact River Ranch at their 24-hour customer service center at 1-800-762-7708.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Gills Onions Voluntarily Recalls One Lot of Diced Red Onions Because of Possible Health Risk
Contact:
Consumer:
1-800-348-2255
Media:
Amy Philpott
703-472-6615
aphilpott@watsonmulhern.com disclaimer icon
FOR IMMEDIATE RELEASE - May 19, 2012 - May 19, 2012-Gills Onions, LLC of Oxnard, CA is initiating a voluntary recall, 2,360 pounds, of diced red onions with lot code 51RDA1A2119 and use-by-dates May 14, 15 and 17, 2012 because it may be contaminated by Listeria monocytogenes. The product is beyond its use-by-date, no illnesses have been reported in connection with this recall, and no other Gills Onions product is affected by this recall.
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled diced red onions were distributed directly from Gills Onions to retailers in Canada and retailers and foodservice distributors in California, Oregon, Washington, Arizona, Idaho, Texas, Illinois, Michigan, Arkansas, Ohio, Tennessee, New Jersey, Georgia, and Florida.
Recalled product sold at retail was packaged in a 7oz. clear plastic clamshell, labeled Gills Onions with the May 17, 2012 use-by-date and the lot code 51RDA1A2119 stamped on the UPC label. The UPC number in Canada is 643550 00045 0 and the UPC number in the United States is 643550 00041 2. However, since this number can also be on other products, please refer to the lot code in order to identify the recalled product. Photos are available on our website. Anyone who has the recalled product in their possession should discard it.
Product sold to foodservice customers was packaged in 5 lb clear plastic bags, identified as Gills Onions Diced Red Onions, and stamped with an expiration date of May 14 or 15, 2012. The lot code 51RDA1A2119 is also stamped on both the bag and box. Photos are available on our website.
This voluntary recall was initiated as a result of a routine and random test directed by the Canadian Food Inspection Agency. Gills Onions has notified all customers who received the recalled lot directly from the company and requested that they remove from commerce any of the expired product they may still have in stock. As an extra precautionary measure and because we do not always know to whom our direct customers sell our products, we are also asking our direct customers to notify their customers of this recall. Gills Onions is keeping the U.S. Food and Drug Administration and the Canadian Food Inspection Agency informed of its recall process to assure that consumers are properly alerted.
Consumers with questions may contact Gills Onions at 1-800-348-2255, M-F 8am-5pm PDT or at 1-209-678-1354 today, Saturday, May 19, 2012. Please visit our website at www.gillsonions.com disclaimer icon for updates.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
River Ranch Expands Salad Recall Because Of Possible Health Risk
Contact:
Consumer:
1-800-762-7708
Media:
Kim St George
831-758-1390
FOR IMMEDIATE RELEASE - May 19, 2012 - River Ranch Fresh Foods, LLC of Salinas, CA is expanding its voluntary recall of retail and foodservice bagged salads, because they have the potential of being contaminated with Listeria monocytogenes.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Retail salad products under this recall were distributed throughout the United States and Canada under various sizes and packaged under the brand names of River Ranch, Farm Stand, Hy-Vee, Shurfresh, and The Farmer’s Market.
Foodservice salad products under this recall were distributed throughout the United States and Canada under various sizes and packaged under the brand names of River Ranch and Sysco.
The recalled retail and foodservice salad bags have either “Best By” code dates between 12MAY2012 – 29MAY2012 or Julian dates of 118 and 125. The code date is typically located in the upper right hand corner of the bags.
See attached list for the specific salad products, size, package type, UPC codes and states of distribution.
No other products, brands or code dates aside from those listed below are affected by this recall.
There have been NO reported illnesses associated with this recall. We are working closely with the Food & Drug Administration and California Department of Public Health.
Consumers who have purchased this product should not consume it and are urged to return it to the place of purchase for a full refund. Consumers with questions can contact River Ranch at their 24-hour customer service center at 1-888-624-2569.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Pacific Coast Fruit Company Recalls Single Side Serving Processed Salads for
Potential Listeria monocytogenes Contamination
Contact:
Consumer:
Pacific Coast Fruit Company
503-234-6411
Media:
Ted Hendryx
503-234-6411
FOR IMMEDIATE RELEASE - May 22, 2012 - Pacific Coast Fruit Company, Portland, Oregon is voluntarily recalling multiple types of bagged processed salads based on the potential contamination of Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Pacific Coast Fruit utilized a portion of the salads that were recalled by River Ranch in some of our retail and food service processed bagged salad. Please see attached list for specific products entered into commerce, including UPC code, Pacific Coast Fruit Item Number, and Best if Use By Date or Production Date.
Pacific Coast recalled products were distributed to Fred Meyer, Avanti, and Evergreen in Oregon, Washington, Alaska and Idaho.
The recalled retail salads are packed in a 9.6oz -10oz clamshell style and VA food service items is packed in 5 lbs – 20 lbs food service salads bags.
There have been NO reported illnesses associated with this recall. This voluntary recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
Consumers who have purchased this product should not consume it and are urged to return it to the place of purchase or destroy the product. Consumer with questions can contact Pacific Coast Fruit at 503-234-6411 between the hours of 8 am-4:30 pm PST Monday to Friday.
See here for list of products: http://www.fda.gov/Safety/Recalls/ucm305123.htm?source=govdelivery
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More bagged salad recalls:
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Salads
Contact
Consumer:
Consumer Response Center, (800) 356-3111
Media:
Marty Ordman
Phone: (818) 874-4834
marty.ordman@dole.com
FOR IMMEDIATE RELEASE - June 22, 2012 - Dole Fresh Vegetables is voluntarily recalling 1,077 cases of bagged salads. The products being recalled are Kroger Fresh Selections Greener Supreme coded N158 211B 1613 KR04 with Use-by date of June 19 and UPC 11110 91039, Kroger Fresh Selections Leafy Romaine coded N158 111B KR11 with Use-by date of June 19 and UPC 11110 91046 and Wal Mart Marketside Leafy Romaine coded N158111B with Use-by date of June19 and UPC code 81131 02781 due to a possible health risk from Listeria monocytogenes. Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported in association with the recall.
The Product Code and Use-by date are in the upper right-hand corner of the package; the UPC code is on the back of the package, below the barcode. The salads were distributed in six U.S. states (Georgia, Kentucky, North Carolina, South Carolina, Tennessee and Virginia).
No illnesses have been reported in association with the recall. This precautionary recall notification is being issued due to an isolated instance in which a sample of Marketside Leafy Romaine salad yielded a positive result for Listeria monocytogenes in a random sample test conducted by the Stateof North Carolina.
No other Wal Mart Marketside, or Kroger Fresh Selections salads are included in the recall. Only the specific Product Codes, UPC codes and June 19, 2012 Use-by date identified above are included in the recall. Consumers who have any remaining product with these Product Codes should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Food Company Consumer Response Center at (800) 356-3111, which is open 8:00 am to 3:00 pm (PDT) Monday - Friday.
Although the product is 3 days past its Use-by date and it is highly unlikely that any product is still available at retail, retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Dole Fresh Vegetables customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is not in the stream of commerce.
Listeria monocytogenes is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
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I wonder what's really being done to prevent on a long term basis all these contaminated foods? where does the contamination begin? unsanitary conditions with workers in the field and/or in the plant itself?
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Dole Fresh Vegetables Announces Precautionary Recall of Limited Number of Salads
Contact
Consumer:
Dole Food Company Consumer Response Center
(800) 356-3111
Media:
Marty Ordman
Phone: (818) 874-4834
marty.ordman@dole.com
FOR IMMEDIATE RELEASE – June 29, 2012 – Dole Fresh Vegetables is voluntarily recalling 2,598 cases of bagged salad. The product being recalled is Dole Hearts of Romaine coded 0540N165112A or B, with Use-by date of June 26 and UPC 7143000956 due to a possible health risk from Listeria monocytogenes. Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported in association with the recall.
The product code and Use-by date are in the upper right-hand corner of the package; the UPC code is on the back of the package, below the barcode. The salads were distributed in nine U.S. states (Alabama, Florida, Georgia, Maryland, North Carolina, Pennsylvania, South Carolina, Tennessee and Virginia).
No illnesses have been reported in association with the recall. This precautionary recall notification is being issued due to an isolated instance in which a sample of Dole Hearts of Romaine salad yielded a positive result for Listeria monocytogenes in a random sample test conducted by the FDA.
No other salads are included in the recall. Only the specific Product Codes, UPC codes and June 26, 2012 Use-by date identified above are included in the recall. Consumers who have any remaining product with these Product Codes should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Food Company Consumer Response Center at (800) 356-3111, which is open 8:00 am to 3:00 pm (PT) Monday - Friday.
Although the product is 3 days past its Use-by date and it is highly unlikely that any product is still available at retail, retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Dole Fresh Vegetables customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is not in the stream of commerce.
Listeria monocytogenes is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Gills Onions Voluntarily Recalls Diced and Slivered Red and Yellow Onions, and Diced Onion and Celery Mix Because of Possible Health Risk
Contact
Media
Amy Philpott
aphilpott@watsonmulhern.com
703-472-6615
Consumer
1-800-348-2255
FOR IMMEDIATE RELEASE - July 18, 2012 - Gills Onions, LLC of Oxnard, CA is initiating a voluntary recall of a single day’s production of diced and slivered red and yellow onions and diced celery and onion mix because they may be contaminated by Listeria monocytogenes. No illnesses have been reported in connection with this recall, and no other Gills Onions products are affected by this recall. A list of recalled products is provided at the end of this release.
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products, which are packaged under the brand "Gill's Onions," were shipped between July 2-4, 2012 directly from Gills Onions to retailers in Canada and the following U.S. states: California, Montana, Oklahoma, Oregon, Pennsylvania, Texas, Utah and Washington.
This voluntary recall was initiated when the company was notified by the U.S. Food and Drug Administration that a random sample of diced yellow onions taken at retail tested positive for Listeria monocytogenes. As a precautionary measure, Gills Onions is recalling all products processed on the same day and on the same line as the sample that tested positive.
Gills Onions is notifying all customers who received the recalled product directly from the company and requesting that they remove it from commerce. We are also asking our direct customers to notify their customers of this recall. Gills Onions is keeping the U.S. Food and Drug Administration informed of its recall process to assure that consumers are properly alerted.
“Gills Onions is committed to protecting public health and to executing this voluntary recall effectively and efficiently,” said Steve Gill, president of the company. “We are a multi generational family business, and we work hard every day to earn the trust and confidence of customers and consumers who enjoy our high quality, healthy products.”
Anyone who has the recalled product in their possession should not consume it and should destroy or discard it. Consumers with questions may contact Gills Onions at 1-800-348-2255, M-F 8am-5pm PDT. Please visit our website at www.gillsonions.com for a copy of this release.
Gills Onions’ July 18, 2012 product recall
Recalled
Lot Code
Product Description
("Gill's Onions” Brand)
Use-by-date
UPC Code*
USA
22YAA1A2184
Diced Yellow Onions, 7 oz
07/20/12
643550000405
22RAA1A2184
Diced Red Onions, 7 oz
07/20/12
643550000412
22YAA1A2184
Slivered Yellow Sweet Onions, 5oz
07/20/12
643550000092
22RAA1A2184
Slivered Red Onions, 5 oz
07/20/12
643550000009
22YAA1A2184
Diced Celery and Onion, 7 oz
07/20/12
643550000429
22YAA1A2184
Diced Celery and Onion, 19 oz
07/20/12
643550000351
CANADA
22YAA1A2184
Diced Yellow Onions,
Oignons jaunes frais, en dés, 198g
07/20/12
643550000443
22RAA1A2184
Diced Red Onions,
Oignons rouge frais, en dés, 198g
07/20/12
643550000450
22YAA1A2184
Diced Celery & Onions,
Céleri et oignons frais, en dés, 198g
07/20/12
643550000467
*The UPC Code can also be found on products not included in this recall, so please refer to the lot code in order to identify the recalled product.
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GH Foods CA Initiates Voluntary Recall of Products That Contain Yellow Onions
07/28/2012 11:46 AM EDT
GH Foods CA, LLC, is initiating a voluntary recall of various products containing yellow onions distributed to retail supermarkets. The products were manufactured using onions recalled by Gills Onions because they have the potential to be contaminated with Listeria monocytogenes.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Simmering Soup Voluntarily Recalls Salsa & Balela
Because of Possible Health Risk
Contact:
Dr. David Nyachuba
davidnyachuba@simmeringsoup.com
401-225-1288
FOR IMMEDIATE RELEASE - July 27, 2012 - Simmering Soup, Inc., Atlanta, GA is initiating a voluntary recall of the following Trader Joe’s brand of Salsa and Balela because the products contain diced onions that are the subject of a U.S. Food and Drug Administration (FDA) recall due to possible Listeria monocytogenes contamination.
Product Description Use-by-date SKU # UPC
Mild Salsa 16 ounce 08/09 082584 00285841
Balela 8 ounce 07/31 068306 00683067
* Packaging: Translucent plastic cups, snap on lids.
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products, which are packaged under the "Trader Joe’s" brand, were shipped between July 25 -26, 2012 to Trader Joe’s stores in the following states: Florida, Georgia, North Carolina, South Carolina, Tennessee, and Southern region of Virginia.
None of these products have tested positive for Listeria and no illnesses have been reported to date. No other Trader Joe’s products produced at the Simmering Soup Atlanta facility are affected by this recall.
This voluntary recall was initiated when the company was notified by FreshPoint Atlanta, which uses Gills Whole Peeled Onions for further processing to produce diced onions purchased by Simmering Soup Atlanta. Listeria was found in the facility in which the Gills Whole Peeled Onions were processed.
Immediately following notification from Simmering Soup, Trader Joe’s removed products affected by this recall from store shelves and destroyed them. Simmering Soup is keeping the U.S. Food and Drug Administration informed of its recall process to assure that consumers are properly alerted.
Anyone who has the recalled product(s) in their possession should not consume it and should destroy, discard it or return it to the place of purchase for a full refund. Consumers with questions may contact Simmering Soup at davidnyachuba@simmeringsoup.com or 401-225-1288, M-F 9am-5pm EST.
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Wegmans Recalls Chilled Prepared Foods that Contain Diced White Onions Sold at Three Pennsylvania Stores Only
07/27/2012 05:04 PM EDT
Wegmans Food Markets, Inc. is recalling prepared foods that contain chopped/diced white onions as an ingredient because the onions have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Huxtable's Kitchen Voluntarily Recalls Trader Joe's brand Roasted Butternut Squash, Red Quinoa and Wheatberry Salad Because of Possible Health Risk
Contact
Consumer:
(323) 923-2885
Media:
Jason Knight
(323) 923-2905
FOR IMMEDIATE RELEASE - July 27, 2012 - Huxtable's Kitchen is initiating a voluntary recall of Trader Joe's Roasted Butternut Squash, Red Quinoa and Wheatberry Salad because the onions used as an ingredient have the potential to be contaminated by Listeria monocytogenes.
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant women.
Trader Joe's Roasted Butternut Squash, Red Quinoa & Wheatberry Salad with "use by date" of 7/28/2012 and 7/30/2012 comes in a 9.5 oz clear plastic container. The "use by date" is marked on a sticker on the front of the package. The recalled product was distributed from 7/23/12 to 7/26/12 to Trader Joe's stores in Arizona, California, Nevada, New Mexico, Oregon and Washington. No other Trader Joe's stores are affected by this recall.
The onions are a product of Gill Onions, Oxnard, CA, which initiated a recall of the onions on July 18, 2012, and were supplied to Huxtable's Kitchen, Inc. Immediately following notification from Huxtable's Kitchen, Inc., Trader Joe's removed affected product from store shelves and destroyed them.
No illnesses have been linked to this recall. Anyone who has the recalled product in their possession should not consume it and should destroy or discard it. Consumers with questions may contact Huxtable’s Kitchen: at 323-923-2885, M-F 8am-5pm PDT.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
North Carolina Farm Recalls Athena Cantaloupes
Contact
Consumer:
Michael Norton:
207-885-3132
FOR IMMEDIATE RELEASE - July 28, 2012 - On Saturday, Burch Farms of North Carolina announced a recall of Athena cantaloupes because the product may contain listeria monocytogenes. No illnesses have been associated with this recall, according to Burch Farms.
Hannaford is advising customers because its stores had carried Burch Farms Athena cantaloupes. The product has been removed. Athena cantaloupes, a variety grown in the Southeastern United States, are a whole cantaloupe produce item. If stickered, the label on the item will reference Burch Farm and read: “Cantaloupe PLU 4319.”
Customers should not consume these cantaloupes. Return the item to stores or dispose of the item and return the sticker for a full refund. Listeria has the potential to cause serious illness.
No other products are affected by this recall.
Hannaford Supermarkets, based in Scarborough, Maine, operates 181 stores and employs more than 26,000 associates in Maine, Massachusetts, New Hampshire, New York and Vermont. For additional information, visit disclaimer icon www.hannaford.com.
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Today is Wednesday and time for another round of recall alerts from the FDA. Gill's Onion contamination caused all of the following recalls.
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Garden Fresh Foods, Inc. Recalls Specific Packages Of Products Containing Onions Because Of Possible Health Risk Due To Gills Onions Expanded Recall
Contact
Consumer:
1-800-645-3367
Media:
Steve Mueller
414-645-1000
FOR IMMEDIATE RELEASE - July 31, 2012 - Garden-Fresh Foods is initiating a voluntary recall on various ready-to-eat salads, slaw, salsa, bean and dip products sold under various brands and code dates (see attachment). The products may contain onions from Gills Onions, which may be contaminated with Listeria monocytogenes, an organism that can cause serious and sometimes-fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Products are sold in various size containers (8oz to 8 pound packages). The product were distributed in the following states: WI, MN, IA, IL, OH, IN, TX, FL, MA, MO, MI, PA, AZ, CA, and distributed to retail stores and food services.
Consumers who have purchased any of the suspect products are urged to return it to the place of purchase for a full refund. Currently there has been no illness reported related to this recall.
Consumers with questions may contact the company at 1-800-645-3367 Monday through Friday between the hours 8:00AM- 4:30 PM
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Ken’s Foods, Inc. Issues Voluntary Recall of a Limited Number of Branded Food Service Dressings and Sauces Containing Onions Because Of Possible Health Risk Due To Gills Onions Recall
Contact
Consumer:
508-229-1100, extension 4727 or 1190
Media:
Joni A Fagan, Vice President of Quality
Ken’s Foods, Inc.
jfagan@kensfoods.com
508-229-1124
FOR IMMEDIATE RELEASE -July 30, 2012 – The manufacturer of Golden Corral Tartar Sauce, Dickey’s BBQ Bean Sauce, Lee’s Cole Slaw Dressing, Fatz Tartar Sauce, Ken’s Tartar Sauce. These items contain onions from Gills Onions, which may have been contaminated with Listeria monocytogenes, an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and still births among pregnant women.
This recall comes as a result of a July 25, 2012, recall issued by Gills Onions, Oxnard, CA a supplier to Fresh Point, Atlanta. Fresh Point further processes the onions for Ken’s Foods, Inc.
The products included in this recall are listed below. No other Ken’s products are affected by this recall. As of this date, there have been no illnesses reported relating to this recall.
KE0666-Ken’s Tartar Sauce 4/1-gallon containers MFG: 09/JUL/12
KE0666A5-Ken’s Tartar Sauce 100/1.5oz cups EXP: 011313
DI2063-Dickey’s BBQ Bean 10/48oz pouches USE BY: 11MAR13
GD2517-Golden Corral Tartar 4/1-gallon containers MFG: 17/JUL/12
FQ2103-Lee’s Cole Slaw 14/40oz pouches MFG: 23JUL12
FD0666-Fatz Tartar Sauce 4/1-gallon containers MFG: 23/JUL/12
On Friday, July 27, 2012, Ken’s Foods, Inc. notified all distribution centers, private label customers and brokers to request immediate withdrawal of potentially affected items listed above. The above listed items were distributed to the states of AL,FL,GA,IL,KY,MS,NC,NE,NM,NV,OH,OK,SC,TN,TX,WI.
If there are any questions pertaining to this notice, please call Ken’s Foods, Inc., Monday through Friday, 9:00am - 5:00pm EST at 1-508-229-1100, ask for extension 4727 or 1190.
###
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Publix Recalls Sub Sandwiches with Onions Due To Possible Health Risk
Contact
Consumer:
1-800-242-1227
1-888-723-3366
Media:
Maria Brous
863-680-5339
FOR IMMEDIATE RELEASE - July 26, 2012 - Publix Super Markets is issuing a voluntary recall for custom sub sandwiches that contain onions because they may be adulterated with Listeria monocytogenes. Publix received notification from their supplier, who receives sliced onions from Gills Onions LLC. This recall involves any custom made sub sandwich with onions sold from the Publix Deli department between July 7, 2012 through July 26, 2012 in Alabama, Georgia, Tennessee, and South Carolina. Publix stores in Florida are not involved with this recall.
Consumption of products containing Listeria monocytogenes can cause serious and sometimes fatal infection in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
No illnesses have been reported to date in connection with the sliced onions.
"As part of our commitment to food safety, potentially impacted product has been removed from all store shelves," said Maria Brous, Publix media and community relations director. "Consumers who have purchased the products in question may return the product to their local store for a full refund. Publix customers with additional questions may call our Customer Care Center at 1-800-242-1227 or by visiting our website at www.publix.com. Customers can also contact the US Food and Drug Administration at 1-888-SAFEFOOD (1-888-723-3366)."
Publix is privately owned and operated by its 152,500 employees, with 2011 sales of $27.0 billion. Currently Publix has 1,055 stores in Florida, Georgia, South Carolina, Alabama and Tennessee. The company has been named one of FORTUNE’s "100 Best Companies to Work For in America" for 15 consecutive years. In addition, Publix's dedication to superior quality and customer service is recognized as tops in the grocery business, most recently by an American Customer Satisfaction Index survey. For more information, visit the company's website, www.publix.com disclaimer icon .
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Spartan Stores Voluntarily Recalls Deli/Produce Products Containing Peeled Whole Yellow Onions
Contact:
1-800-451-8500
1-888-220-0436
FOR IMMEDIATE RELEASE - July 26, 2012 – Grand Rapids, Michigan – Spartan Stores today is announcing the voluntary recall of two (2) products processed between the dates of July 13 through July 26, 2012 that contain onions produced by Gills Onions of Oxnard, California. The recall is in connection with an expanded voluntary recall announced by Gills Onions, LLC., of their Peeled Whole Yellow Onions due to possible contamination with Listeria Monocytogenes. The products being voluntarily recalled are:
• Deli – Three Bean Salad
• Produce – 10 oz. Broccoli Stir Fry
Spartan Stores has received no confirmation of illness associated with the consumption of these products. Anyone concerned about an illness should contact their healthcare provider immediately.
All of the products involved in the recall should be discarded or returned for a full refund or replacement.
Consumers with questions about the recall may contact Spartan Stores’ Consumer Affairs at 1-800-451-8500 or contact Gills Onions Customer Service at 888-220-0436.
About Spartan Stores
Grand Rapids, Michigan-based Spartan Stores, Inc. (Nasdaq: SPTN) is the nation's tenth largest grocery distributor with 1.4 million square feet of warehouse, distribution, and office space located in Grand Rapids, Michigan. The Company distributes more than 40,000 private and national brand products to approximately 375 independent grocery locations in Michigan, Indiana and Ohio, and to our 97 corporate owned stores located in Michigan, including Family Fare Supermarkets, Glen's Markets, D&W Fresh Markets, VG's Food and Pharmacy, and Valu Land.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Stop & Shop Alerts Customers to Voluntary Recall of Calico Bean Salad
Item Sold on Salad Bar
Contact
Consumer:
1-800-322-1374
1-800-343-0836
1-800-767-7772
Media:
Susan Liner
NWE-DO Recall Coordinator
Phone: 781-587-7481
Fax: 781-587-7556
Email: susan.liner@fda.hhs.gov
FOR IMMEDIATE RELEASE - July 27, 2012 - The Stop & Shop Supermarket Company LLC, following a recall by Costa Fruit & Produce, announced it removed from sale Calico Bean Salad, sold on the salad bar, due to a possible health risk of listeria monocytogenes.
No illnesses have been reported to date. Customers who have purchased the product between July 18, 2012 and July 26, 2012 should discard any unused portions and bring their purchase receipt to Stop & Shop for a full refund.
Listeria is a common organism found in nature. Consumption of food contaminated with Listeria monocytogenes can cause listeriosis, an uncommon but potentially fatal disease. Healthy people rarely contract listeriosis. However, listeriosis can cause high fever, severe headache, neck stiffness and nausea. Listeriosis can also cause miscarriages and stillbirths, as well as serious and sometimes fatal infections in those with weakened immune systems, such as infants, the elderly and persons with HIV infection or undergoing chemotherapy.
Consumers in Massachusetts looking for additional information on the recall may call Costa Fruit & Produce at 1-800-322-1374, all other consumers may call 1-800-343-0836 or visit Costa Fruit & Produce's website at www.freshideas.com disclaimer icon . Customers may also call Stop & Shop customer service at 1-800-767-7772 or visit the Stop & Shop website at www.stopandshop.com disclaimer icon .
About Stop & Shop
The Stop & Shop Supermarket Company employs approximately 62,000 associates and operates more than 400 stores throughout Massachusetts, Connecticut, Rhode Island, New Hampshire, New York, and New Jersey. The company helps support local communities fight hunger, combat childhood cancer and promote general health and wellness - with emphasis on children's educational and support programs. In its commitment to be a sustainable company, Stop & Shop is a member of the U.S. Green Building Council and EPA's Smart Way program; has been awarded LEED (EB) certifications for 50 of its existing stores; and has been recognized by the EPA for the superior energy management of its stores. Stop & Shop is an Ahold company. To learn more about Stop & Shop, visit www.stopandshop.com disclaimer icon .
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Burch Equipment LLC Expands Cantaloupe Recall Due to Possible Health Risk
Contact:
Consumer:
910-267-5781
burch@intrstar.net
FOR IMMEDIATE RELEASE - August 2, 2012 - Burch Equipment LLC, North Carolina is expanding their recall that was initiated on July 28th, 2012. The firm is voluntarily recalling 13888 cases of whole Athena variety cantaloupes ( 9 cantaloupes per case) and 581 bins ( 110 cantaloupes per bin) of Athena variety cantaloupes due to the potential for being contaminated with Listeria monocytogenes. Melons affected by this recall total 188,902.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The whole Athena variety cantaloupes were shipped between July 15th and July 27th and distributed to retail stores operating in FL, GA, IL, MD, NC, NJ, NY, PA, SC and VA. The whole cantaloupes are identified by a red label reading Burch Farms referencing PLU # 4319. All cantaloupes involved in the recall were grown by Burch Farms, however some of the cantaloupes may have been identified with a "Cottle Strawberry, Inc." sticker referencing PLU #4319. Cottle Farms is not involved in this recall. The Athena variety cantaloupe is the most commonly grown in the east. Cantaloupes from Burch Farms were shipped to retail establishments in both corrugated boxes (9 cantaloupe per case) and in bulk bins.
Burch Equipment LLC is requesting any consumer that may have one of these cantaloupes to discard the product.
There have been no illnesses reported to date. FDA and the North Carolina Department of Agriculture are working with Burch Equipment LLC following a random sample of an Athena variety cantaloupe testing positive for Listeria monocytogenes. The recall expansion is based on unsanitary conditions found at the cantaloupe packing shed during FDA’s ongoing inspection that may allow for contamination of cantaloupes with Listeria monocytogenes.
Questions can be directed to Burch Equipment LLC at 910 267 5781 Monday through Friday, (9:00am to 4:00pm) or email burch@intrstar.net.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Burch Equipment LLC Corrects Cantaloupe Variety Subject to Recall
Contact:
Consumer:
910-267-5781
burch@intrstar.net
FOR IMMEDIATE RELEASE - August 3, 2012 - Burch Equipment LLC, North Carolina, is correcting the variety of cantaloupe involved in recalls initiated on July 28 and August 2, 2012. Previous announcements incorrectly identified the cantaloupes as being the Athena variety. The cantaloupes affected by the recall are the Caribbean Gold variety.
Athena cantaloupes are not subject to the recall.
Today’s announcement is not an expansion of the recall; no additional products are being recalled at this time.
The firm voluntarily recalled 580 cases of cantaloupes on July 28, and voluntarily recalled an additional 13,888 cases of cantaloupes (9 cantaloupes per case) and 581 bins of cantaloupes (110 cantaloupes per bin) on August 2, due to the potential for being contaminated with Listeria monocytogenes. Melons affected by this recall total 188,902.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The whole Caribbean Gold variety cantaloupes were shipped between July 15th and July 27th and distributed in FL, GA, IL, MD, ME, NC, NJ, NY, PA, SC and VA. The whole cantaloupes are identified by a red label reading Burch Farms referencing PLU # 4319. All cantaloupes involved in the recall were grown by Burch Farms, however some of the cantaloupes may have been identified with a "Cottle Strawberry, Inc." sticker referencing PLU #4319. Cottle Farms is not involved in this recall. Cantaloupes from Burch Farms were shipped in both corrugated boxes (9 cantaloupe per case) and in bulk bins.
Burch Equipment LLC is requesting any consumer that may have one of these cantaloupes to discard the product.
There have been no illnesses reported to date. FDA and the North Carolina Department of Agriculture and Consumer Services are working with Burch Equipment LLC following a random sample of a Caribbean Gold variety cantaloupe testing positive for Listeria monocytogenes. The recall expansion was based on unsanitary conditions found at the cantaloupe packing shed during FDA’s ongoing inspection that may allow for contamination of cantaloupes with Listeria monocytogenes.
Questions can be directed to Burch Equipment LLC at 910-267-5781 Monday through Friday, (9:00am to 4:00pm) or email burch@intrstar.net.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Reichel Foods, Inc. Issues Voluntary Recall For Dippin' Stix Sliced Apples & Caramet with Peanuts and Armour Active Packs Cheese Pizza Lunch Kits Because of Possible Health Risk
Contact
Consumer:
866-372-2609
www.reichelfoods.com
Media:
Karin Grzanek
866-372-2609
FOR IMMEDIATE RELEASE - August 6, 2012 - Reichel Foods, Inc. of Rochester, Minnesota is voluntarily recalling a limited amount of Dippin’ Stix Sliced Apples & Caramel with Peanuts and Armour Active Packs Cheese Pizza Lunch Kits because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
No illnesses have been reported to date.
Product was distributed to retail and convenience stores throughout the United States.
The products subject to recall are:
2.75 oz. single serve trays of Dippin’ Stix Apples & Caramel with Peanuts. The affected case code dates are 09/01/12, 09/02/12, and 09/03/12. The affected single serve tray code dates are USE BY 01SEP2012, USE BY 02SEP2012, and USE BY 03SEP2012.
5.6 oz. packages of “Armour Active Packs Cheese Pizza” Package Code 1026090112 or Case Code 27815-17996.
The problem was discovered through microbiological testing by Reichel Foods. The company has not received reports of illnesses due to consumption of these products. Anyone concerned about an illness should contact a healthcare provider.
Consumers who have purchased any products with the code dates listed above should dispose of this product immediately or return it to the place of purchase for a full refund. Consumers with questions may contact Reichel Foods at (866) 372-2609 (7:00 am to 4:30 pm CST) or visit the company website at www.reichelfoods.com.
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Recall -- State / Local Press Release
FDA posts press releases and other notices of recalls and safety alerts from states as a service to consumers, the media, and other interested parties. FDA is not responsible for the content of these notices.
HEALTH Advises Consumers Not to Eat Certain Food Products From Target Stores
Contact
Consumer:
800-645-3367
Target Guest Relations:
800-440-0680
Target.com Guest Services:
800-591-3869
Media:
Dara Chadwick
401-222-3998
FOR IMMEDIATE RELEASE - August 7, 2012 - The Rhode Island Department of Health (HEALTH) advises consumers that they should not eat certain foods from the Market Pantry and Archer Farms Deli Salad lines. The products are sold at Target stores, and are being voluntarily recalled because they may be contaminated with Listeria monocytogenes.
Consumers who have purchased the following items should discard them immediately:
Target Item Number (DPCI):
216-24-0207, Archer Farms Four Bean Salad 14-oz
216-24-0102, Market Pantry American Potato Salad 3#
216-24-0107, Market Pantry American Potato Salad 16 oz
216-24-0103, Market Pantry Chicken Salad 12-oz
216-24-0106, Market Pantry Cole Slaw, 15-oz
216-24-0114, Market Pantry Cole Slaw, 44-oz
216-24-0109, Market Pantry Egg Salad, 12-oz
216-24-0101, Market Pantry Macaroni Salad 3#
216-24-0105, Market Pantry Macaroni Salad 16-oz
216-24-0104, Market Pantry Mustard Potato Salad 16-oz
216-24-0100, Market Pantry Mustard Potato Salad 3#
216-24-0116, Market Pantry Reduced Fat Mustard Potato Salad 16-oz
216-24-0108, Markel Pantry Tuna Salad 12-oz
216-24-0119, Market Pantry Italian Pasta Salad 14-oz
878-02-0051/0151 Layered Taco Dip
There are several date codes for each item. Consumers should refer to the item list at Garden-Fresh Foods-Market Pantry and Archer Farms Deli Salad items for specific date and code information.
Not all Target stores carried the recalled items or the recalled date codes.
Specific questions regarding lhis recall should be directed to Garden-Fresh Foods, which manufactured the products. Consumers may call (800) 645-3367. Consumers can also contact Target Guest Relations for in-store purchases at (800)-440-0680 and Target.com Guest Services for online purchases at (800) 591-3869.
Symptoms of listeriosis can include high fever, severe headache, stiffness and nausea, or abdominal pain and diarrhea. Anyone who has eaten these products and experiences these symptoms should contact their healthcare provider.
No illnesses have been reported in connection with these products at this time.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Missa Bay, LLC Announces Voluntary Recall Of Fruit, Vegetable, and Sandwhich
Products Containing Apples Because of Possible Health Risk
Contact
Consumer
1‐800‐800‐7822
Media
Tristan Simpson
Corporate Communications
626‐678‐2055
FOR IMMEDIATE RELEASE - August 10, 2012 - Missa Bay, LLC, a wholly owned subsidiary of Ready Pac Foods, Inc., of Swedesboro, New Jersey is voluntarily recalling a total of 293,488 cases and 296,224 individually distributed units of fruit, vegetable, and sandwich products containing apples, as listed below, with the Use‐by dates of July 8, 2012 through August 20, 2012 because they contain diced or sliced apples which may be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism that can cause serious or life‐threatening food borne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastro intestinal symptoms such as nausea or diarrhea. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
The recalled products were produced and distributed from the Missa Bay, LLC facility to retailers and foodservice operators in the following states: Alabama, Arkansas, Connecticut, Delaware, District of Columbia, Washington D.C., Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Mississippi, Montana, Nebraska, New Hampshire, New Jersey, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Vermont, Virginia, Wisconsin and West Virginia.
This recall notification is being issued due to finding Listeria monocytogenes on equipment used by Missa Bay, LLC to produce apple products. Missa Bay, LLC is coordinating closely with regulatory officials. No illnesses have been reported in association with this voluntary recall.
Only the specific products identified in the list below are included in the recall. Retailers and foodservice operators should check their inventories and store shelves to confirm that none of the product is present or available for purchase by consumers or in warehouse inventories.
Consumers who may have purchased the affected product are asked to record the Use‐by date and/or UPC code number, immediately dispose of the product, and contact the Ready Pac Consumer Affairs Department, toll‐free at (800) 800‐7822, Monday – Friday, 8 a.m. to 5 p.m. (Pacific Time) to obtain a full refund. Please visit our website at www.readypac.com disclaimer icon for a copy of the release.
Ready Pac Foods, Inc. has earned an outstanding safety record for over 40 years and has taken immediate precautionary measures to protect public health by issuing this voluntary recall. Ready Pac customer service representatives have already contacted all customers impacted and are in the process of confirming that the recalled products are not in the stream of commerce. Consumers with questions may contact Ready Pac directly at 1‐800‐800‐7822 M‐F 8am‐5pm PDT.
Missa Bay, LLC August 10, 2012 Precautionary Voluntary Recall
Alabama, Arkansas, Connecticut, Delaware, District of Columbia, Washington D.C., Florida, Georgia, Iowa, Illinois, Indiana, Kentucky, Louisiana, Maine, Maryland, Massachusetts, Michigan, Minnesota, Missouri, Mississippi, Montana, Nebraska, New Hampshire, New Jersey, New York, North Carolina, North Dakota, Ohio, Oklahoma, Pennsylvania, Rhode Island, South Carolina, South Dakota, Tennessee, Vermont, Virginia, Wisconsin and West Virginia.
Go here for long list of products: http://www.fda.gov/Safety/Recalls/ucm315249.htm?source=govdelivery
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Dole Fresh Vegetables Announces Recall Of Limited Number Of Salads
Contact
Consumer:
(800)-356-3111
Media:
Marty Ordman
(818) 874-4834
marty.ordman@dole.com
FOR IMMEDIATE RELEASE - August 22, 2012 - Dole Fresh Vegetables is voluntarily recalling 1,039 cases of bagged salad. The product being recalled is 10 oz. Dole Italian Blend coded 0049N2202008, with a Use-By date of August 20 and UPC 7143000819 due to a possible health risk from Listeria monocytogenes. Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported in association with the recall.
The product code and Use-By date are in the upper right-hand corner of the package; the UPC code is on the back of the package, below the barcode. The salads were distributed in eight U.S. states (Florida, Alabama, North Carolina, South Carolina, Pennsylvania, Maryland, Mississippi and Virginia). No illnesses have been reported in association with the recall. This recall notification is being issued due to an isolated instance in which a sample of Dole Italian Blend salad yielded a positive result for Listeria monocytogenes in a random sample test conducted by the North Carolina Department of Agriculture.
No other salads are included in the recall. Only the specific product codes, UPC codes and August 20, 2012 Use-By date identified above are included in the recall. Consumers who have any remaining product with this Product Code should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Food Company Consumer Response Center at (800) 356-3111, which is open 8:00 a.m. to 3:00 p.m. (PT) Monday-Friday.
Although the product is 2 days past its Use-By date and it is highly unlikely that any product is still available at retail, retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Dole Fresh Vegetables customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is not in the stream of commerce.
Listeria monocytogenes is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Fresh Express Recalls Limited Quantity of Expired 10 oz. Hearts of Romaine Salad Due to Possible Health Risk
Contact:
Consumer:
800-242-5472
Media:
Tiffany Breaux
704-280-5938
Barbara Hines
972-724-3049
FOR IMMEDIATE RELEASE - August 26, 2012 - Fresh Express Incorporated is voluntarily recalling a limited quantity of expired 10 oz. Hearts of Romaine salad with the expired Use-by Date of August 23, 2012 and a Product Code beginning with "G222" as a precaution due to a possible health risk from Listeria monocytogenes.
No illnesses are reported in association with the recall. No other Fresh Express products are being recalled.
Fresh Express customer service representatives are already contacting retailers to confirm the product was removed from their inventories and store shelves in accordance with standard procedures for products that have reached their expiration date. Customers with questions may contact their Fresh Express customer service representative.
In an unlikely event that consumers may still have this expired product in their refrigerators, it should not be consumed, but discarded instead. Consumers with questions may call the Fresh Express Consumer Response Center at (800) 242-5472 during the hours of 8 a.m. to 7 p.m. Eastern Daylight Time.
The precautionary recall notification for the now-expired salad is being issued due to an isolated incident in which a sample of a singled package of 10 oz. Hearts of Romaine salad yielded a positive result for Listeria monocytogenes as part of the U.S. Food and Drug Administration’s random sample testing program. Fresh Express is continuing to coordinate closely with regulatory officials.
The limited quantity of recalled product is identified with a Product Code beginning with "G222" and a Use-by Date of August 23, which is located in the upper right-hand corner of the package. In addition, the UPC Code of 71279 26102 is located on the back of the package below the barcode. The 10 oz. Hearts of Romaine was distributed in limited quantities to predominantly eastern and southeastern states.
Listeria monocytogenes is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. If it spreads to the nervous system symptoms may include headache, stiff neck or confusion. The illness primarily affects pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
###
Note:
The expired Fresh Express Hearts of Romaine salads being recalled display a use-by date of August 23, 2012 with a Product Code beginning with G222.
BRAND PRODUCT NAME SIZE PKG TYPE UPC POSSIBLE DISTRIBUTION STATES
Fresh Express Hearts of Romaine 10 oz Bag 7127926102 AL, AR, FL, GA, IL, IN, KY, LA, MD, MO, MS, NC, OH, PA, SC, TN, TX, VA, WV
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Manna Organics Recalls Tofu and Sprouts Because of Possible Health Risks
Contact:
Consumer:
Sun Ja Lee
862-267-3400
FOR IMMEDIATE RELEASE August 31, 2012 - Manna Organics, Inc. of Newark, NJ, is recalling various soybean sprouts and tofu products listed in the table below because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products were distributed to various restaurants, retailers, and distributors in NY, NJ, PA, MA, VA, MD, CT, GA, IL, and TX on or after July 17, 2012.
The Jinga Firm and Soft, SooNyeoWon Firm and Soft Tofu are packaged in a square 16-ounce white plastic container with the label sealed on top with UPC Codes: 0 28346 09112 4, 0 28346 09111 7, 0 28346 07812 5 and 0 28346 07814 9. Expiration date of September 9, 2012 or later is printed in black on top of the label.
The 5 pieces and 10 pieces tofu are packaged in a white plastic bucket. The 5 pieces and 10 pieces are lidded and labeled in Korean "Healthy Tofu" with UPC Codes 0 28346 09125 4 and 0 28346 09129 2. Affected products have an expiration date of July 25, 2012 or later.
The Soy Milk is packaged in a 1.3 gallon white plastic pail.
The Large Tofu Bucket(30 pieces), Soon tofu, and Small Tofu are packaged in a large, white plastic pail enclosed in a plastic bag labeled TOFU with the company name, address, and nutritional information listed directly below. Affected products have an expiration date of July 25, 2012 or later.
SooNyeoWon Silken Tofu is packaged in a small 14-ounce square plastic container with the label sealed on top. It has a UPC Code of 0 28346 09113 1. There is an expiration date printed in black on top of the label. Affected products have an expiration date of September 9, 2012 or later.
The Soybean Sprouts 16-ounce products come in a clear plastic sealed bag colored in red or green with the labels SOONYEOWON SOYBEAN SPROUTS or SOONYEOWON HEALTHY SOYBEAN SPROUTS with UPC Codes 0 28346 07121 8 and 0 28346 07140 9. The Soybean Sprouts 10lbs. and 5 lbs. bags come in a clear hand tied plastic poly bag labeled SPROUTS with the company info directly beneath it.
See link for list of products: http://www.fda.gov/Safety/Recalls/ucm317996.htm?source=govdelivery
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I understand how raw spinach, lettuce, and sprouts are infected, but how is it that soy milk and tofu which is cooked is infected? This the first time I have seen this. Cooking does not remove the risk of Mad Cow Disease or Scrapie cancer, but bacteria ought to be killed. It must be in the packaging process which leads one to wonder how is that we are seeing such contamination. What happened to safety standards? Are these products coming from China or are they processed in the US? We need to know.
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Yes, we do and this most recent recall is very troubling.
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Water could also be the key to this. Here is an older report:
http://www.aquaox.net/uploads/EAW_in_Tofy_Manufacturing.pdf
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Whole Foods Market recalls cheese in 21 states and Washington, D.C.
because of possible health risk
Contact:
Consumer:
512-542-0060
FOR IMMEDIATE RELEASE - September 12, 2012 - Whole Foods Market announces that it is recalling ricotta salata sold in 21 states and Washington, D.C. that came from its supplier Forever Cheese Inc. of Long Island City, NY. Forever Cheese recalled this cheese product because it may be contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled Ricotta Salata Frescolina brand cheese was cut into wedges, packaged in clear plastic wrap and sold with a Whole Foods Market scale label using PLU 293427. All “sell by” dates through Oct. 2 are affected. Fourteen illnesses have been reported which may be associated with the Frescolina recall.
Whole Foods Market stores in the following states are affected by this recall:
1. Alabama (1 store)
2. Arizona (2 stores)
3. California (2 stores)
4. Colorado(2 stores)
5. Florida (5 stores)
6. Georgia (4 stores)
7. Kansas (1 store)
8. Kentucky (1 store)
9. Maryland (6 stores)
10. North Carolina (7 stores)
11. New Jersey (2 stores)
12. New Mexico (2 stores)
13. New York (2 stores)
14. Ohio (2 stores)
15. Oregon (6 stores)
16. Pennsylvania (5 stores)
17. South Carolina (1 store)
18. Tennessee (3 stores)
19. Utah (1 store)
20. Virginia (6 stores)
21. Washington (6 stores)
22. Washington, D.C. (3 stores)
Signage is posted in Whole Foods Market stores to notify customers of this recall. Customers who have purchased this product from Whole Foods Market may return it to the store for a full refund, and call with questions 512-542-0060 Monday through Friday, 8:00 a.m. to 5:00 p.m. Central Standard Time.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Kroger Stores in Fifteen States Ask Customers to Check for
Recalled Fresh Selections Spinach Items
Contact:
Consumers:
1-800-KROGERS
Media:
Keith Dailey
1-513-762-1304
Investors:
Cindy Holmes
1-513-762-4969
FOR IMMEDIATE RELEASE - September 19, 2012 - The Kroger Co. (NYSE:KR) Family of Stores in 15 states is asking customers to check their refrigerators for certain Kroger Fresh Selections Tender Spinach 10 ounce packages (UPC: 0001111091649) with a "best if used by" date of September 16.
This product, supplied by NewStar Fresh Foods LLC, is being recalled because the product may contain Listeria monocytogenes. Customers should return the items to stores for a full refund or a replacement. Customers can visit www.kroger.com/recall for more information.
Stores under the following names in 15 states are included in this recall:
Kroger stores in Ohio, Kentucky, West Virginia, Virginia, Georgia, Alabama, North Carolina, South Carolina, central and eastern Tennessee, and Michigan.
Kroger, Jay C, Owen’s, Pay Less, Scott’s and Food 4 Less stores in Indiana, Illinois and eastern Missouri.
Dillons, Baker’s, and Gerbes stores in Kansas, Missouri, and Nebraska.
Stores the company operates under the following names are not included in this recall: Fry’s, Ralphs, Fred Meyer, QFC, Smith’s, King Soopers, City Market and Food 4 Less/Foods Co. in California.
What Kroger is Doing
Kroger has removed affected items from store shelves and initiated its customer recall notification system. Customers who may have purchased the affected products will receive register receipt messages and/or automated phone calls. Kroger is also placing signs in stores in produce departments.
What Customers Should Do
Kroger is asking customers to carefully check their refrigerators for this recalled Fresh Selections product because it may contain Listeria monocytogenes. Any opened or unopened products included in this recall should not be consumed and should be returned by customers to their local Kroger store for a full refund or replacement.
Listeria monocytogenes, if eaten, could result in severe illness to those individuals who are pregnant or have a weakened immune system.
Customers with additional questions can contact 1-800-KROGERS.
Kroger, one of the world's largest retailers, employs more than 339,000 associates who serve customers in 2,425 supermarkets and multi-department stores in 31 states under two dozen local banner names including Kroger, City Market, Dillons, Jay C, Food 4 Less, Fred Meyer, Fry's, King Soopers, QFC, Ralphs and Smith's. The company also operates 788 convenience stores, 342 fine jewelry stores, 1,124 supermarket fuel centers and 37 food processing plants in the U.S. Recognized by Forbes as the most generous company in America, Kroger supports hunger relief, breast cancer awareness, the military and their families, and more than 30,000 schools and grassroots organizations in the communities it serves. Kroger contributes food and funds equal to 160 million meals a year through more than 80 Feeding America food bank partners. For more information please visit Kroger.com.
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Publix Hearts of Romaine (http://links.govdelivery.com/track?type=click&enid=ZWFzPTEmbWFpbGluZ2lkPTIwMTIwOTI4LjEwODI3NTkxJm1lc3NhZ2VpZD1NREItUFJELUJVTC0yMDEyMDkyOC4xMDgyNzU5MSZkYXRhYmFzZWlkPTEwMDEmc2VyaWFsPTE2OTU3OTgzJmVtYWlsaWQ9c3liaWxAbmV3bWV4aWNvLmNvbSZ1c2VyaWQ9c3liaWxAbmV3bWV4aWNvLmNvbSZmbD0mZXh0cmE9TXVsdGl2YXJpYXRlSWQ9JiYm&&&100&&&http://www.fda.gov/Safety/Recalls/ucm321496.htm?source=govdelivery)
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Forever Cheese Recall (http://links.govdelivery.com/track?type=click&enid=ZWFzPTEmbWFpbGluZ2lkPTIwMTIxMDAzLjEwOTM1NzExJm1lc3NhZ2VpZD1NREItUFJELUJVTC0yMDEyMTAwMy4xMDkzNTcxMSZkYXRhYmFzZWlkPTEwMDEmc2VyaWFsPTE2OTYwNTUxJmVtYWlsaWQ9c3liaWxAbmV3bWV4aWNvLmNvbSZ1c2VyaWQ9c3liaWxAbmV3bWV4aWNvLmNvbSZmbD0mZXh0cmE9TXVsdGl2YXJpYXRlSWQ9JiYm&&&100&&&http://www.fda.gov/Safety/Recalls/ucm322347.htm?source=govdelivery)
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Dole - Salads (http://links.govdelivery.com/track?type=click&enid=ZWFzPTEmbWFpbGluZ2lkPTIwMTIxMDE3LjExMjk4NDUxJm1lc3NhZ2VpZD1NREItUFJELUJVTC0yMDEyMTAxNy4xMTI5ODQ1MSZkYXRhYmFzZWlkPTEwMDEmc2VyaWFsPTE2OTY4ODU5JmVtYWlsaWQ9c3liaWxAbmV3bWV4aWNvLmNvbSZ1c2VyaWQ9c3liaWxAbmV3bWV4aWNvLmNvbSZmbD0mZXh0cmE9TXVsdGl2YXJpYXRlSWQ9JiYm&&&100&&&http://www.fda.gov/Safety/Recalls/ucm324315.htm?source=govdelivery)
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ATTENTION Veggie Burger eaters!!!!!!!!
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
VEGGIE PATCH® Voluntarily Recalls Two Items- The Ultimate Meatless Burger and Falafel
- Due To Possible Risk Of Contamination By Listeria monocytogenes
Contact
Consumer:
888-807-0765
contactus@veggiepatch.com
Media:
Laura Herbert
212-219-0321
herbert@formulapr.com
FOR IMMEDIATE RELEASE – November 30, 2012 – VEGGIE PATCH® is voluntarily recalling two products --The Ultimate Meatless Burger and Falafel-- due to a risk of contamination with Listeria monocytogenes. Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy persons may suffer only short-term symptoms such as high fever, severe headaches, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths in pregnant women.
The Ultimate Meatless Burger and Falafel, from VEGGIE PATCH, with the specific use-by dates and UPC codes listed below were distributed to a select number of retailers and distributors.
9-ounce trays of refrigerated, fully cooked, VEGGIE PATCH, The Ultimate Meatless Burger with a Use-By date, Jan/12/2013; UPC code 6-10129-00211-5 (which can be found on back of package)
9-ounce trays of refrigerated, fully cooked, VEGGIE PATCH, Falafel with a Use-By date, Jan/15/2013; UPC code 6-10129-06619-3 (which can be found on back of package)
The Ultimate Meatless Burger potentially affected was available for sale as of November 21, 2012, in the following states; NY, CT, PA, FL, IL, MD, IN, WI, VA, NJ and DE. Falafel potentially affected, was available for sale as of November 21, 2012, nationwide.
No illnesses have been reported to date. VEGGIE PATCH discovered this issue as part of its routine testing of its products.
Consumers who purchased any product with the specific use-by dates and UPC codes listed above are asked to dispose of the product. They should email contactus@veggiepatch.com to arrange for a full refund. The recall affects only these two items. Products that do not contain the specific use-by dates and UPC codes listed are not affected by the recall. No other VEGGIE PATCH products or other use-by dates of The Ultimate Meatless Burger or Falafel are affected by this recall. Frozen Veggie Patch products are not affected by this recall.
Consumers with questions can contact VEGGIE PATCH at 888-807-0765, 8am- 5pm EST, seven days a week, or at contactus@veggiepatch.com
More information is available on the VEGGIE PATCH website at www.veggiepatch.com
About VEGGIE PATCH
VEGGIE PATCH offers tasty, healthy and convenient vegetarian foods and meatless options ideal for snacks, lunch and dinner. Products include main dish items, kid-friendly vegetable and cheese bites and other appetizers. All VEGGIE PATCH products are made from real vegetables, are high in protein and free of trans fats and MSG. For more information, visit http://www.veggiepatch.com disclaimer icon
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Followup recall:
Recall - Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Stop & Shop alerts customers to voluntary recall of Veggie Patch Ultimate Meatless Burgers
Contact:
Consumer:
1-888-698-3444
800-767-7772
Media:
Arlene Putterman
203‐551‐2464
cservice@verathon.com
Suzi Robinson
617-774-4434
suzi.robinson@stopandshop.com
FOR IMMEDIATE RELEASE - November 30, 2012 - The Stop & Shop Supermarket Company LLC, following a recall by Veggie Patch, announced it removed from sale packages of ultimate meatless burgers due to possible contamination by Listeria monocytogenes.
The following product is included in this recall:
Veggie Patch Ultimate Meatless Burger, UPC 61012900211, 9 oz., sell by date of January 12, 2013
Stop & Shop has received no reports of illnesses to date. Customers who have purchased the product should discard any unused portions and bring their purchase receipt to Stop & Shop for a full refund.
Listeria is a common organism found in nature. Consumption of food contaminated with Listeria monocytogenes can cause listeriosis, an uncommon but potentially fatal disease. Healthy people rarely contract listeriosis. However, listeriosis can cause high fever, severe headache, neck stiffness and nausea. Listeriosis can also cause miscarriages and stillbirths, as well as serious and sometimes fatal infections in those with weakened immune systems, such as infants, the elderly and persons with HIV infection or undergoing chemotherapy.
Consumers looking for additional information on the recall may call Veggie Patch customer service at 1‐888‐698‐3444. In addition customers may call Stop & Shop Customer Service at (800) 767‐7772 for more information. Customers can also visit the Stop & Shop website at www.stopandshop.com.
About Stop & Shop
The Stop & Shop Supermarket Company LLC employs approximately 62,000 associates and operates more than 400 stores throughout Massachusetts, Connecticut, Rhode Island, New Hampshire, New York, and New Jersey. The company helps support local communities fight hunger, combat childhood cancer and promote general health and wellness – with emphasis on children’s educational and support programs. In its commitment to be a sustainable company, Stop & Shop is a member of the U.S. Green Building Council and EPA’s Smart Way program; has been awarded LEED (EB) certifications for 50 of its existing stores; and has been recognized by the EPA for the superior energy management of its stores. Stop & Shop is an Ahold company. To learn more about Stop & Shop, visit www.stopandshop.com.
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Sliced apples recall: FCA Recalls (http://www.fda.gov/Safety/Recalls/ucm331564.htm?source=govdelivery)
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Salinas Firm Conducts Precautionary Recall On A Select Salad Product Due To Possible Health Risk
Contact
Consumers/Media:
866-508-7048
FOR IMMEDIATE RELEASE - December 13, 2012 - Taylor Farms Retail, Inc. of Salinas is initiating a precautionary recall of 110 cases of Taylor Farms Hearts of Romaine 10 oz. bags with an expiration date of 12-13-12. This product is being recalled out of an abundance of caution following a single random finished package test conducted by the Food and Drug Administration (FDA) which tested positive for Listeria monocytogenes. There have been no complaints or illnesses reported in association with this recall. No other Taylor Farms products or brands are included in this recall.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Details of the recalled product are as follows:
Brand Item Description UPC Number Package Code Best By State
Taylor Farms Hearts of Romaine,10 oz. bag 0 30223 04032 3 TFRS332A09 12-13-12 CA, FL
The “Best By” Code Date for the recalled products can be located on the top/middle right portion of the front label.
The company is cooperating with the Food and Drug Administration (FDA) and California Department of Public Health (CDPH) regarding this recall.
Customers who have purchased this product are urged not to consume the product and should dispose of it. Consumers may contact Taylor Farms Retail, Inc. for further information at 866-508-7048 Monday through Friday 8 am to 5 pm PST. Consumers with concerns about an illness from consumption of this product should contact a health care provider.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Sprouter Northwest Recalls Alfafa, Brocco Sandwich Sprouts, Clover, Spicy Sprouts Because of Possible Health Risk
Contact:
Joe Campbell
Consumer:
1-253-872-0577
FOR IMMEDIATE RELEASE - January 28, 2013 - Sprouters Northwest of Kent, Washington is recalling 1953 pounds of alfalfa, clover, brocco sandwich sprouts, and spicy sprouts due to the potential contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
Products were distributed from 1/10/13 to 1/18/13 in Washington, Oregon, Alaska, and British Columbia, Canada through retail stores and food service distribution chain.
The affected products are sold under the Sprouters Northwest brand and are packaged in plastic clamshell containers and plastic 1 lb bags.
Click here for list of products: http://www.fda.gov/Safety/Recalls/ucm337098.htm?source=govdelivery
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
UPDATED--Sprouters Northwest Expands Voluntary Recall to All Varieties of Sprouts Products, Wheatgrass, and Pea Shoots Because of Possible Health Risk
Contact
Consumers
Joe Campbell
(253)872-0577
FOR IMMEDIATE RELEASE - February 6, 2013 - Sprouters Northwest is voluntarily recalling all varieties of sprouts products, wheatgrass and pea shoots due to the potential contamination with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women. There have been no illnesses reported to date.
All varieties of sprouts products including 3-Bean Munchie, Alfalfa, Bean, Broccoli, Brocco Sandwich sprouts, Clover, Deli, Spicy; Wheatgrass and Pea Shoots that were distributed through 1/30/2013 in Alaska, Idaho, Oregon, Washington, and British Columbia, Canada through retail stores and food service distribution chain.
The affected products are sold under the Sprouters Northwest, LifeForce and Brassica brand names and are packaged in plastic clamshell containers, plastic cups, plastic trays in 3 oz., 4 oz., 5 oz., and in plastic 1 lb. 2lb, or 5lb. bags. The Best by Dates are including all and up to 2/17/2013. Trader Joe's Organic Pea Shoots (SKU 92756), packaged in a 4 oz. clamshell offered only in Oregon and Washington state are also affected. The Best by Dates are through 02/16/13. The Best by Date sticker is located in the top right hand corner, front of the package.
The problem was identified through surveillance finished products samples collected at retail locations and at the firm by the Washington State Department of Agriculture. Sprouters Northwest is working with WSDA and the Food & Drug Administration on this recall.
Consumers who have purchased a specific lot of items mentioned above are urged to return it to the place of purchase for a full refund or dispose of it. Consumers with questions may contact the Sprouters Northwest at 1-253-872-0577 from 7AM to 2PM PST.
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I just contacted the company to see if there is something being done to eliminate this problem that continues to pop up with sprouts, among other vegetable products. e. coli is one of the infectious agents that also is very worrisome that has been found in sprouts.
It is often the case that when attempting to get information that is important, companies begin to question those who are seeking important information. The company representative wanted to know who I was. Since the information I was seeking, what is being done to prevent these infections of food stuff, has nothing to do with who I am, I expressed this. The rep would not continue the conversation. This is worrisome also.
Often there is no public reporting that we can see as to what caused the problem. Since it is a matter of life and death to some, there is a responsibility to the public to inform us as to what caused the product to be infected and what is being done to make sure it does not happen in the future.
We will continue to recommend that bagged lettuce, spinach, and sprouted products be viewed with great concern. Sprouts are a healthy food, but not when infected by the food producer. The largest outbreak of e coli occurred recently in Europe. 53 deaths were confirmed and over 4,000 made sick from sprouted seeds which were infected with e. coli bacteria. e. coli (http://remnant-online.com/smf/index.php?topic=3204.80) The sprouting process opens the door to bacterial infections by providing a perfect growing environment if the bacteria is present.
We are sympathetic to the problem this presents for the responsible grower/producer, but until the industry takes steps to insure the safety of the public, I will not buy these products. The refusal of the producer in this case to discuss the matter only causes greater concern.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Hagee Foods Inc. dba Penny's Salsa Inc. Recalls Hummus Products Because of Possible Health Risk
Contact:
Consumer:
(866) 797-2572
FOR IMMEDIATE RELEASE - July 16, 2013 - Hagee Foods Inc. dba Penny's Salsa Inc., is recalling hummus products listed in the attached table because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
The retail hummus products come in 8 oz. and 12 oz. clear plastic packages and were distributed to retail stores and food service accounts in Oregon and Washington with the Penny's Salsa, Tacoma Boys and Harbor Greens labels. The USE BY dates 7/13/2013-8/25/2013 are printed on the side of the top lid.
Vegetable trays 8 oz and Snack packs 8 oz, which include 1.5 oz plastic containers of creamy hummus labeled Made in the Pacific North West, are packaged in black plastic trays with clear plastic lids. These products were distributed in Oregon and Washington. The USE BY dates 7/13/2013-7/24/2013 are on the underside of these trays.
Hummus for foodservice is packaged in 25 lb. bulk boxes. USE BY dates 7/13/2013-8/25/2013 are printed on the master shipper labels. This product was distributed in Washington.
The above hummus products were shipped from 5/27/13 to 7/14/13. No illnesses have been reported to date in connection with these products.
The potential for contamination was noted after routine testing by the Washington State Department of Agriculture (WSDA) revealed the presence of Listeria monocytogenes in 12 ounce containers of Hummus.
The production of the product has been suspended while FDA, WSDA and the company continue to investigate the source of the problem.
Consumers who have purchased any size of Penny's Salsa Hummus are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company at 1-866-797-2572.
UPC Number Product
7 49404 83061 4 Penny's Garlic Hummus 12 oz (340 g)
7 49404 90971 6 Penny's Creamy Hummus 12 oz (340 g)
7 49404 32368 0 Penny's Hummus De Gallo 12 oz (340 g)
7 49404 51848 2 Penny's Roasted Red Pepper Hummus 12 oz (340 g)
7 49404 91368 3 Penny's Jalapeño Hummus 12 oz (340 g)
7 49404 70200 3 Penny's Black Bean Hummus 12 oz (340 g)
7 49404 80515 5 Harbor Greens Black Bean Hummus 8 oz (227g)
7 49404 80717 3 Harbor Greens Sun-Dried Tomato Hummus 8 oz (227g)
7 49404 80313 7 Harbor Greens Jalapeño Hummus 8 oz (227g)
7 49404 80414 1 Harbor Greens Roasted Red Pepper Hummus 8 oz (227g)
7 49404 80616 9 Harbor Greens Hummus De Gallo 8 oz (227g)
7 49404 80212 3 Harbor Greens Garlic Hummus 8 oz (227g)
7 49404 90515 2 Tacoma Boys Black Bean Hummus 8 oz (227 g)
7 49404 90414 8 Tacoma Boys Roasted Red Pepper Hummus 8 oz (227g)
7 49404 90313 4 Tacoma Boys Jalapeño Hummus 8 oz (227g)
7 49404 90717 0 Tacoma Boys Sun Dried Tomato Hummus 8 oz (227g)
7 49404 90212 0 Tacoma Boys Garlic Hummus 8 oz (227g)
7 49404 90616 6 Tacoma Boys Hummus De Gallo 8 oz (227g)
7 49404 98020 3 Vegetable tray 8 OZ. Ingredients: Carrot Sticks, Celery, Grape Tomatoes, Creamy Hummus
7 49404 30002 5 Vegetable tray 8 OZ. Ingredients: Carrot Sticks, Pretzels, Grapes, Creamy Hummus
07494041923679 Penny's Salsa Inc. Snack Pack w/Hummus Grapes, Carrots and Pretzels 8 oz
07494041923606 Penny's Salsa Inc. Snack Pack w/Hummus Celery, Carrots, Tomato 8 oz
No UPC Penny's Salsa Creamy Original Hummus 25 LB
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Heeren Brothers Recalls Cantaloupe Because of Possible Health Risk
Contact
Consumer:
616-452-2101
Media:
Mary Ann Sabo
616-485-1432
FOR IMMEDIATE RELEASE - Grand Rapids, Michigan, August 6, 2013 - Heeren Brothers Produce is recalling approximately 5,400 cantaloupes because of a possible health risk to consumers.
The produce, which was distributed to small, independent grocers in Michigan July 23-26, has the potential to be contaminated with Listeria monocytogenes and should be discarded and not consumed. The cantaloupes are Athena Cantaloupes, but have no stickers or other markings that identify them as such.
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, the elderly or others with weak immune systems. Healthy individuals may suffer short-term symptoms, such as high fever, severe headache, stiffness, nausea, abdominal pain or diarrhea. Listeria can cause miscarriages and stillbirths in pregnant women.
Heeren Brothers Produce has not received any case of reported illnesses related to this product to date. The recall does not affect any other Heeren Brothers Produce products.
Heeren Brothers Produce became aware of this issue after the Food & Drug Administration conducted a routine sampling and found the cantaloupes contained the bacteria.
After receiving notice from the FDA, Heeren Brothers Produce immediately alerted retailers and requested that they remove the produce from their shelves. Heeren Brothers Produce has also contacted the supplier of the cantaloupes. The source of the potential issue is still under investigation. Heeren Brothers Produce is cooperating fully with the FDA.
Heeren Brothers Produce is committed to consumer safety. We have product handling and safety protocols in place to assure that we provide our retailers and their customers with fresh, safe and healthy products. A recent audit by an independent, third-party laboratory rated our procedures as excellent in the industry.
Consumers who have questions may contact Heeren Brothers Produce at 616.452.2101 Monday through Friday from 8 a.m. to 5 p.m.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Buurma Farms, Inc. Recalls Fresh Cilantro Due to Possible Health Risk
Contact:
Consumer:
Joel Buurma, 419-935-6411
Media:
Dr. Karl Kolb 715-723-4915
FOR IMMEDIATE RELEASE August 16, 2013 – August 17, 2013, Willard, OH – Buurma Farms, Inc. is voluntarily recalling 465 boxes of Cilantro Lot #02D312A4. Buurma Farms recalled this product due to possible Listeria monocytogenes contamination, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Buurma Farms, Inc. has not received any case of reported illness related to this product to date.
The Cilantro was sold to distributors in Michigan on August 3, 2013. The product was also shipped to retail stores in Illinois, Indiana, Michigan and Ohio. The Cilantro, which was distributed through Meijer and Ben B Schwartz and Sons in Michigan the week of August 5-9, could be contaminated with Listeria monocytogenes. The Cilantro has a Buurma Farms twist-tie on it.
Product affected by the recall is:
Cilantro, fresh, UPC #4889, Lot #02D312A4, GTIN: 0 33383 80104 9
Product is sold in ~4 oz. bunches with a Product of USA Buurma Farms #4889 labeled twist tie,
Consumers who may have purchased this product should return or dispose of the product.
Buurma Farms Inc. became aware of this issue after the Michigan Department of Agriculture conducted a routine test on a sample obtained at Ben B Schwartz and found that sample contained the bacteria. The recall does not affect any other Buurma Farms produce products.
Upon learning of the potential contamination, Buurma Farms quickly alerted the retailer and wholesaler and requested they remove the produce from their shelves. The source of the contamination is still under investigation. To date Buurma Farms has not been able to find any other evidence of contamination within their supply chain. Buurma Farms, Inc. is fully co-operating with the FDA in its investigation.
Buurma Farms Inc. is committed to consumer safety. We have product handling and food safety protocols in place to assure we provide our retailers, wholesalers, and their customers with fresh, safe, and healthy products. Our audits by an independent third party laboratory rated our procedures as superior in the industry.
Customers who have questions may contact Buurma Farms Inc. at 419-935-6411, Monday through Friday 8 am to 5 pm Eastern. A list of possible retailers who may have received this product is listed below.
See list here: http://www.fda.gov/Safety/Recalls/ucm365422.htm
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The FDA press release on this recall lists the retail stores that received the product, and their addresses. This is very good, but seldom do we see this. It is not the company, but the FDA that makes the decision. When health and life are at risk, this ought to be done every time there is a recall. For those of you who have not seen the list, if you eat fresh cilantro and live in Michigan, Ohio, or Illinois, you need to take a look at the list.
I am following up to find out why we got the addresses this time and seldom do at other times. This is a real problem when there is a recall of food possibly contaminated with E. coli or even Mad Cow Disease. They will not reveal the store addresses from what I have read. There are considerations more important than the health and life of the consumer.
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Praise the Lord it was posted here. We had cilantro that was to be served in our cafeteria today that was purchased from Meijer. It could have affected our entire class on the first day of school, but we caught it in time because I saw the recall here. Thanks for posting.
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Thank the Lord! Whew! I am so happy to know this.
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Little do we know sometimes how little actions of love can have great results.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Garden-fresh Foods, Inc. Recalls Spartan Fresh Selection American Potato Salad in 16 Oz. Packages Because of Possible Health Risk
Contact:
Consumer:
1-800-645-3367
Media:
Robert Clark 1-414-645-1000
FOR IMMEDIATE RELEASE August 30, 2013 – Garden-Fresh Foods, Inc. of Milwaukee Wisconsin is recalling A Limited Quantity of Spartan Fresh Selections American Potato Salad In 16 oz. Packages, because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Spartan Fresh Selections American Potato Salad was distributed by Spartan Stores in the State of Michigan and Toledo Ohio.
The affected Spartan Fresh Selections American Potato Salad is packaged in square 16 oz. plastic retail containers with a UPC Code Number 0 11213 90320 0 and a USE BY DATE of 09/06/13/04.
There have been no illnesses reported in connection with this product.
The potential for contamination was noted after routine testing revealed the presence of Listeria monocytogenes in 16 oz. packages of Spartan Fresh Selections American Potato Salad with a USE BY DATE OF 09/06/13/04.
Consumers who have purchased this product should not open the package or use the contents. Instead, they should return the product to the location of purchase for a full refund.
Consumers with questions can contact Garden-Fresh Foods, Inc. at 1-800-645-3367 Monday through Friday between the hours of 8:00 a.m. and 4:00 p.m.
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This is a large recall. Go to the website to see the long list. FDA (http://www.fda.gov/Safety/Recalls/ucm371955.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery)
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Reser’s Fine Foods, Inc. Recalls Refrigerated Ready-to-Eat Products Due to Potential Health Risk
Contact
Consumer:
1-888-257-7913
www.resers.com
Media:
Steve Loehndorf
800-333-6431
FOR IMMEDIATE RELEASE - October 22, 2013 - Reser’s Fine Foods of Beaverton, Oregon is recalling approximately 109,000 cases of refrigerated ready-to-eat products because it may be contaminated with Listeria monocytogenes. Listeria is an organism which can cause serious and sometime fatal infections in young children, frail or elderly people and individuals with weakened immune systems. Healthy people may suffer only short term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea. Listeria infection can cause miscarriages and stillbirths among pregnant woman.
The recalled refrigerated ready-to-eat products were distributed nationwide and Canada.
The product is sold in retail and food service establishments. The packages will be marked with a Use-by-Date or Best By Date and followed by a plant identifier code of 20. Products affected by this recall are listed below.
NO illnesses have been reported to date.
The recalled products were manufactured at the Topeka, KS salad manufacturing facility. No other Reser’s Fine Foods, Inc. manufacturing facilities are involved in this recall.
Consumers who purchased the product may take it back to the store for a refund or discard it.
For more information please contact Reser’s Fine Foods Consumer Hotline 1-888-257-7913 (8am-8pm EST) or visit the FDA website: www.fda.gov.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Tennessee and Maryland Firms Initiate Recall Based on Reser's Fine Foods Recall
Contact:
Consumer:
(866) 508-7048
FOR IMMEDIATE RELEASE - October 25, 2013 - Following the Reser's Fine Foods, Inc. ("Reser's") recall where select Reser's products were recalled due to the potential of being contaminated with Listeria monocytogenes, Taylor Farms Tennessee, Inc. ("TFTN") and Taylor Farms Maryland, Inc. ("TFMD") are voluntarily recalling a limited number of products that contain Reser's recalled ingredients. There have been no reported illnesses associated with these products. The products subject to the recall were only served at the deli counters at the respective establishments listed below and are limited to the code dates provided. These products are being recalled because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women. To date, there have been no reported illnesses associated with these recalled items.
For list of broccoli items recalled, click here. (http://www.fda.gov/Safety/Recalls/ucm372471.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery)
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Garden Fresh Foods, Inc. Expands Recalls on Specific Packages of Products Because of Possible Health Risk
Contact:
Consumer:
1-800-645-3367
Steve Mueller
414- 645-1000
FOR IMMEDIATE RELEASE - September 26, 2013 - Garden-Fresh Foods is initiating an expansion to our voluntary recall on various ready-to-eat salads, slaw, and dip products sold under various brands and code dates (see attachment). The products may be contaminated with Listeria monocytogenes, an organism that can cause serious and sometimes-fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Products are sold in various size containers (2 lb to 5 lb containers). The products were distributed in the following states: WI, MN, IA, IL, OH, IN, TX, FL, MA, MO, MI, PA, AZ, CA, and distributed to retail stores and food services.
Consumers who have purchased any of the suspect products are urged to return it to the place of purchase for a full refund. Currently there has been no illness or complaints related to this recall.
Consumers with questions may contact the company at 1-800-645-3367 Monday through Friday between the hours 8:00AM- 4:30 PM
Products in this recall. (http://www.fda.gov/Safety/Recalls/ucm372751.htm)
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It appears that most of this is processed foods that most likely include animal products, mayo, eggs, milk.
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No doubt.
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This is a sizable recall. Click on the link below to view the products affected.
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Garden-Fresh Foods, Inc. Expands Recall Due to Potential Contamination with Listeria Monocytogenes
Contact
Consumer:
1-800-645-3367
FOR IMMEDIATE RELEASE - November 7, 2013 - Garden-Fresh Foods has initiated an expansion of previous recalls of fresh cut vegetables, ready-to-eat salads, slaws, dips and spreads sold under various brands and code dates manufactured prior to November 06, 2013. All packaging types and sizes are included. The company has not received reports of illnesses due to consumption of these products, however anyone concerned about an illness should contact a healthcare provider.
The products may be contaminated with Listeria monocytogenes, an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The products were sold nationwide to retail stores, restaurants and institutions. Garden-Fresh Foods Inc. is concerned that expired product may be frozen in consumer homes. Consumers who have purchased these products are urged to return them to the place of purchase for a full refund.
Consumers with questions may contact the company at 1-800-645-3367 Monday through Friday between the hours 8:00AM - 4:30 PM.
Go to List (http://www.fda.gov/Safety/Recalls/ucm374295.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery)
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Crunch Pak Issues Voluntary Recall of
Limited Quantities of Crunch Pak Brand Apple Slices
Because of Possible Health Risk
Contact
Consumer:
1-509-888-7648
Customerservice@crunchpak.com
Media:
Amy Philpott
202-384-1840
aphilpott@watsongreenllc.com
FOR IMMEDIATE RELEASE - November 14, 2013 - Crunch Pak® of Cashmere, Washington is voluntarily recalling 5,471 cases of Crunch Pak® Apple Slices due to a possible health risk from Listeria monocytogenes.
No illnesses have been reported in association with this recall to date. No other Crunch Pak® products are affected by this recall. FDA is aware that the company is undertaking this voluntary action.
Listeria monocytogenes is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The company sold the recalled product to retail customers and because, in some cases, the recalled product was shipped to regional distribution centers, Crunch Pak is taking the extra precautionary measure of issuing this recall nationwide to assure that consumers who may have purchased the product are properly alerted.
The following products are subject to this nationwide recall
Product Description for Nov. 14, 2013 Voluntary Recall Totaling 5,471 cases
UPC Code *
Best if Used By Date*
Crunch Pak® Tart Apple Slices 14 ounce bag
732313141209
11/14/13
Crunch Pak® Tart Apple Slices 2 ounce bag with Low Fat Caramel Dip Multi pak of 5
732313091139
11/14/13
Crunch Pak® Tart Apple Slices 2 ounce bag Multi pak of 6
732313121034
11/14/13
Crunch Pak® Tart Apple Slices 3 pound bag
732313481206
11/14/13
Crunch Pak® Sweet Honeycrisp Apple Slices 12 ounce bag
732313120013
11/14/13
Crunch Pak® Blue Raspberry Flavorz Apple Slices 2 ounce bag Multi pak of 5 with Monsters University
732313089969
11/18/13
* In order to identify the recalled products, both the product description or UPC code AND the Best-if-Used-By-Date must be used. The UPC code and best by date are printed on the back of the packages. Because the UPC code is used for all items in these categories, the UPC code alone will not identify the recalled product.
Consumers who have recalled product in their possession should not consume it, should destroy or discard it, and retain the receipt of purchase. Consumers with questions may contact Crunch Pak at 1-509-888-7648, M-F, 8:00am – 5:00 p.m. Pacific Standard Time. For a copy of this press release and photos of the recalled products, please visit www.crunchpak.com disclaimer icon .
This voluntary recall was initiated after a single, random sample of 14 oz. package of Crunch Pak brand Tart Apple Slices, taken by the Minnesota Department of Agriculture, tested positive for Listeria monocytogenes.
Crunch Pak representatives are already contacting retail customers who received the product directly from the company and asking that they remove the recalled product from store shelves and inventories and that no product is available for consumer purchase.
“We are issuing this voluntary recall to reduce even the slightest risk to public health. There is nothing more important than the health and safety of those who enjoy our products,” said Tony Freytag of Crunch Pak. “We have always been committed to food safety, and we will continue to make food safety a core competency of our company. We realize that food safety is a constant effort, and we are using this opportunity to further evaluate our food safety systems.”
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Spokane Produce, Inc. Voluntarily Recalls Victor™ Toasted Sesame Hummus Because Of Possible Health Risk
Contact:
Consumer:
Dan Petek
1-509-710-8301
dpetek@mac.com
FOR IMMEDIATE RELEASE - December 20, 2013 -Spokane Produce, Inc., of Spokane Washington is recalling approximately 59 lbs of Victor’s Sesame Hummus due to concerns about possible Listeria Monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
The following product is subject to the voluntary recall:
11oz labeled “Victor™ - Toasted Sesame Hummus” with UPC 6 09722 76501 5, best by 12/29/13.
The hummus was distributed to retail locations (Rosauers, Brewster Market, SuperOne) in Washington and Montana.
No illnesses have been reported in association with this recall.
Listeria Species were discovered during routine testing of the newly released product. The listeria test utilized is an indicator of several species of listeria and does not specifically indicate listeria monocytogenes.
Consumers who have purchased Victor™ - Toasted Sesame Hummus are urged not to eat it and to dispose of it or return it to the place of purchase for a full refund.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Dole Fresh Vegetables Voluntarily Recalls Limited Number of Bagged Salads Due to Possible Health Risk
Contact:
Consumer:
800-356-3111
Media:
William Goldfield
818-874-4647
William.Goldfield@Dole.com
FOR IMMEDIATE RELEASE - March 13, 2014 - Dole Fresh Vegetables is voluntarily recalling a limited number of cases of bagged salad. The products being recalled are Dole Italian Blend (UPC 7143000819), Fresh Selections Italian Style Blend (UPC 1111091045), Little Salad Bar Italian Salad (UPC 4149811014) and Marketside Italian Style Salad (UPC 8113102780) coded A058201A or B, with Use-by date of March 12, 2014 due to a possible health risk from Listeria monocytogenes. Dole Fresh Vegetables is coordinating closely with regulatory officials. No illnesses have been reported in association with the recall.
The product code and Use-by date are in the upper right-hand corner of the package; the UPC code is on the back of the package, below the barcode. The salads were distributed in 15 U.S. states (Connecticut, Florida, Illinois, Indiana, Kentucky, Maryland, Massachusetts, Michigan, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Virginia) and 3 Canadian provinces (New Brunswick, Ontario & Quebec).
No illnesses have been reported in association with the recall. This precautionary recall notification is being issued due one sample of Dole Italian salad which yielded a positive result for Listeria monocytogenes in a random sample test conducted by the Canadian Food Inspection Agency.
Although product is 1 day past its Use-By date and it is highly unlikely that any product is still available at retail, retailers should check their inventories and store shelves to confirm that none of the product is mistakenly present or available for purchase by consumers or in warehouse inventories. Dole Fresh Vegetables customer service representatives are already contacting retailers and are in the process of confirming that the recalled product is being removed from the stream of commerce.
Listeria monocytogenes is an organism that can cause foodborne illness in a person who eats a food item contaminated with it. Symptoms of infection may include fever, muscle aches, gastrointestinal symptoms such as nausea or diarrhea. The illness primarily impacts pregnant women and adults with weakened immune systems. Most healthy adults and children rarely become seriously ill.
No other salads are included in the recall. Only the specific Product Codes, UPC codes and March 12, 2014 Use-by date identified above are included in the recall. Consumers who have any remaining product with these Product Codes should not consume it, but rather discard it. Retailers and consumers with questions may call the Dole Food Company Consumer Response Center at (800) 356-3111, which is open 8:00 am to 3:00 pm (PT) Monday - Friday.
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It is not uncommon to find disease in bagged salads. We continue to warn against purchasing them.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Helados La Tapatia, Inc. Recalls Products Because of Possible Health Risk
Contact:
Consumer:
(559) 441-1105
Monday - Friday 6:00 a.m. - 5:00 p.m. (PDT)
Saturday, 9:00 a.m. - 5:00 p.m. (PDT)
Email: helatapatia@sbcglobal.net
After March 20, 2014
(855) 893-1171
FOR IMMEDIATE RELEASE - March 19, 2014 - Helados La Tapatia, Inc., of Fresno, California, is voluntarily recalling all ice cream products, popsicles, fruit bars/cups and bolis due to a possible health risk from Listeria monocytogenes. Helados La Tapatia, Inc., is coordinating closely with regulatory officials.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The products were distributed in Arizona, California, Nevada, Washington, Guam and Canada in retail stores. The products are sold under the brand names of Helados La Tapatia and Icesations.
No illnesses have been reported to date. The recall was the result of a routine inspection program by the U.S. FDA which revealed the presence of the bacteria on certain food processing equipment.
A separate UPC Inventory of the products and their UPC codes is provided.
The production of the products has been suspended while FDA and the company continue to investigate the source of the problem. Consumers who have purchased the Helados La Tapatia or Icesations products are urged to return the products to the place of purchase for a full refund. Consumers with questions may contact the company at 1-559-441-1105 Monday through Friday, 6:00 a.m.- 5:00 p.m. (PDT); Saturday, 9:00a.m.- 5:00p.m. (PDT). After March 20, 2014, a toll free number (1-855-893-1171) will be available. Consumers can also contact the company at helatapatia@sbcglobal.net.
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Recall -- State Press Release
FDA posts press releases and other notices of recalls and safety alerts from states as a service to consumers, the media, and other interested parties. FDA is not responsible for the content of these notices.
Parkers Farm Acquisition, LLC Issues Voluntary Recall of Products Due to Listeria Contamination
Contact
Consumer:
800-869-6685
Media:
Margaret Hart, margaret.hart@state.mn.us,
651-201-6131
FOR IMMEDIATE RELEASE - March 22, 2014 - The Minnesota Department of Agriculture (MDA) is alerting consumers to avoid eating certain peanut butter, cheese, salsa, and spreads produced by Parkers Farm Acquisition, LLC of Coon Rapids, Minnesota, after state agriculture department product sampling determined some of the finished products to be contaminated with Listeria monocytogenes bacteria.
There have been no reports of illness associated with consumption of the products. Parkers Farm Acquisition, LLC is cooperating with the MDA investigation and has issued a voluntary recall of all products with the “sell by” dates listed below. Consumers who have purchased these products are urged to return them to the place of purchase or discard them.
The list of recalled products includes:
16-ounce Parkers peanut butter in square plastic containers (tub with snap-on lid), including creamy, crunchy, honey creamy and honey crunchy varieties with a sell by date before 3/20/2015;
34-ounce Parkers peanut butter in round plastic containers (tub with snap-on lid), including creamy and crunchy varieties with a sell by date before 3/20/2015;
12-ounce Parkers spreads in round or square plastic containers (tub with snap-on lid), including jalapeño and pimento varieties with a sell by date before 9/20/2014;
8-ounce and 16-ounce Parkers cold pack cheese in round plastic containers (tub with snap-on lid), including sharp cheddar, bacon, onion, smoked cheddar, Swiss almond, horseradish, garlic, port wine, and “Swiss & cheddar” varieties with a sell by date before 3/20/2015;
16-ounce Parkers salsa in round plastic containers (tub with snap-on lid), including hot, mild, garlic, and fire-roasted varieties with a sell by date before 7/20/2014;
10-ounce Parkers cheese balls or logs (plastic overwrap), including sharp cheddar, port wine, ranch, and “smokey bacon” varieties with a sell by date before 3/20/2015;
10-ounce Happy Farms cheese balls (plastic overwrap), including sharp cheddar and port wine varieties with a sell by date before 3/20/2015;
16-ounce Happy Farms cold pack cheese in round plastic containers (tub with snap-on lid), including sharp cheddar and port wine varieties with a sell by date before 3/20/2015;
8-ounce Central Markets cold pack cheese in round plastic containers (tub with snap-on lid), including sharp cheddar, port wine, horseradish, and Swiss almond varieties with a sell by date before 3/20/2015;
12-ounce and 20-ounce Hy-Top cheese spread in round plastic containers (tub with snap-on lid), including pimento and jalapeño varieties with a sell by date before 9/20/2014;
8-ounce Amish Classic cold pack cheese in round plastic containers (tub with snap-on lid), including sharp cheddar, port wine, and Swiss almond varieties with a sell by date before 3/20/2015;
14-ounce Say Cheez beer cheese in round plastic container (tub with snap on lid), including regular and hot varieties with a sell by date before 3/20/2015;
10-ounce Win Schuler original variety cheese balls or logs (plastic overwrap) with a sell by date before 3/20/2015;
8-ounce,12-ounce, and 14-ounce Bucky Badger cheese spreads (tub with snap-on lid) including cheddar, port wine, bacon, garlic, horseradish, jalapeño, and Swiss almond varieties with a sell by date before 3/20/2015; and
5-pound foodservice products including cold pack cheese foods, cheese spreads and peanut butter with a sell by date before 3/20/2015.
The products are distributed nationwide under the Parkers Farm, Parkers, Happy Farms, Central Markets, Hy-Top, Amish Classic, Say Cheez, Win Schuler, and Bucky Badger labels. These products were sold at several retail stores including but not limited to Hy-Vee, Cub, Rainbow, Byerly’s, Lunds, Target, Whole Foods, Price Chopper, Nash Finch, Costco, ALDI, Wal-Mart, and Brookshire stores. Consumers with questions can contact the company at (800) 869-6685 or the website: www.parkersfarm.com.
Consumption of food contaminated with Listeria monocytogenes can cause listeriosis, an uncommon but potentially serious disease marked by fever, severe headache, neck stiffness, and nausea. Healthy people rarely contract listeriosis, but it can sometimes cause fatal infections in infants, the elderly, and those with weakened immune systems. Listeriosis can also lead to miscarriages and stillbirths in pregnant women.
Any consumers who believe they may have become ill after eating the products should contact their health care provider.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Oscar’s Smokehouse, Inc. Recalls “Eleven Varieties (11) Of Cheese Spreads” Because of Possible Health Risk
Contact:
Consumer:
1-800-627-3431
Jerold Quintal
518-623-3431
FOR IMMEDIATE RELEASE - March 26, 2014 - Oscars Smokehouse Inc. of Warrensburg, New York is recalling eleven (11) of its 7-oz. “CHEESE SPREADS” varieties marked with 3 digit lot numbers ranging from” 719-959” because they have the potential to be contaminated with Listeria monocytogenes:
-JALAPENO PEPPER CHEDDAR SPREAD, NET WT 7 OZS.
-CHEDDAR SPREAD & BLUE CHEESE, NET WT 7 OZS.
-CHAMPAGNE CHEDDAR SPREAD, NET WT 7 OZS.
-GARLIC CHEDDAR SPREAD, NET WT 7 OZS.
-PORT WINE CHEDDAR SPREAD, NET WT 7 OZS. -TANGY HORSERADISH CHEDDAR SPREAD, NET WT 7 OZS.
-PLAIN CHEDDAR SPREAD, NET WT 7 OZS.
-“MORE THAN” CHEDDAR SPREAD, NET WT 7 OZS.
-HICKORY SMOKED CHEDDAR SPREAD, NET WT 7 OZS.
-BACON & HORSERADISH CHEDDAR SPREAD, NET WT 7 OZS.
-BACON CHEDDAR SPREAD, NET WT 7 OZS.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products were distributed nationwide through mail order sales, wholesale sales and one retail store between 3/21/2013 to 3/21/2014.
The product comes in a 7 oz., clear plastic container marked with lot numbers 719-959 on the bottom of the container or on the cheese spread label itself.
NO ILLNESSES HAVE BEEN REPORTED TO DATE IN CONNECTION WITH THIS PROBLEM.
The potential for contamination was noted after routine testing by the MINNESOTA DEPARTMENT of AGRICULTURE (MDA) revealed the presence of Listeria monocytogenes in 15 products, which included the 5.5lb.package of CHEESE SPREAD BASE produced by PARKERS FARM ACQUISITION, LLC that was used to further manufacture the above mentioned Oscar’s Smokehouse Cheese Spreads.
The production of this product has been suspended while the FDA and PARKER FARM continue to investigate the source of the problem.
Consumers who have purchased any of the 7-oz. “CHEESE SPREAD” products are urged to return them to the place of purchase for a full refund. Customers with any questions may contact Oscar’s Smokehouse, Inc. at 1-800-627-3431, Monday-Sunday 8am-6pm, EST.
This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Sherman Produce Recalls Bulk and Packaged
Walnuts Due to Possible Health Risk
Contact
Consumer:
314-231-2896
FOR IMMEDIATE RELEASE - May 21, 2014 - St. Louis-based Sherman Produce is voluntarily recalling walnuts comprising of 241 cases of bulk walnuts packaged in 25 lb bulk cardboard boxes and Schnucks brand 10 oz trays with UPC 00338390032 with best by dates 03/15 and 04/15 because the products are potentially contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
These products were sold to retailers in MO and IL from March – May 2014.
No illnesses have been reported to date.
The recall was initiated after FDA sampling detected Listeria monocytogenes in walnuts sampled at the facility. All walnuts processed in the facility during the same timeframe as the product found positive are being recalled.
Consumers who have purchased walnuts are urged not to consume them. Consumers are advised to dispose of them or return them to the place of purchase for a full refund. Consumers with any questions may call Sherman Produce at 314-231-2896, 8:30 a.m. to 5 p.m. CST weekdays.
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More walnut recalls:
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Sun Tree LLC Recalls 12oz Packaged California Grown Shelled Walnuts Due to Possible Health Risk
Contact
Glen Kerby
Consumer:
623-707-5604
FOR IMMEDIATE RELEASE - May 23, 2014 - Sun Tree LLC is voluntarily recalling walnuts comprising of 46 cases of 24 count 12oz produce bags, California Grown Shelled Walnuts, Lot No. 42720, Best by 12/11/2014 UPC code, 69887507806, because it has been determined that there is a possibility of contaminated with Listeria monocytogenes. Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
These products were sold to retailers in Kansas City KS in March of 2014.
No illnesses or customer complaints have been reported to date.
The voluntary recall was initiated after FDA sampling detected Listeria monocytogenes in walnuts from a California supplier, Golden State Foods, that also supplied the walnuts that were packed for retail in Kansas City, KS. Even though third party lab testing of product packed did not reveal any harmful pathogen, in cooperating with FDA and for care of our customers we are participating in this voluntary recall. All walnuts processed in the facility during the same timeframe as the product found positive are being recalled to ensure the highest degree of public safety.
Consumers who have purchased walnuts are urged not to consume them. Consumers are advised to dispose of them or return them to the place of purchase for a full refund. Consumers with any questions may call Glen Kerby at (623)-707-5604, 8:30a.m. to 5 p.m. CST weekdays.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Belleville Farmer’s Market Recalls Shelled Walnuts Because of Possible Health Risk
Contact
Consumer:
618-235-9500
FOR IMMEDIATE RELEASE - May 23, 2014 - Belleville Farmer’s Market of Belleville, IL is recalling its packages of Shelled Walnuts because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled Shelled Walnuts were distributed in our Belleville retail stores.
The product comes in an 8 ounce, clear plastic package marked with a Farmer’s Market label indicating pack dates from March 2014 through May 2014.
No illnesses have been reported to date in connection with this problem.
The recall was initiated after FDA sampling detected Listeria monocytogenes in walnuts sampled from a supplier. All walnuts processed in the supplier’s facility during the same timeframe as the product found positive are being recalled.
Consumers who have purchased 8 ounce packages of Shelled Walnuts are urged to return them to 1901 N. Belt West for a full refund. Consumers with questions may contact the company at 1-618-235-9500.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Lansal, Inc. Voluntarily Recalls Egg White Salad With Chives Due To Possible Health Risk
Contact:
Consumer:
1-877-907-7508
Media:
Karen Silverberg
1-847-288-9183 ext. 135
FOR IMMEDIATE RELEASE - June 8, 2014 - Prepared foods manufacturer, Lansal, Inc.(d.b.a. Hot Mama’s Foods), announced today that as a precaution it is voluntarily recalling 304 containers (approximately 114 pounds) of Trader Joe’s Egg White Salad with Chives packaged in 6-ounce plastic containers due to concerns about possible Listeria monocytogenes, an organism, which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled Egg White Salad with Chives was distributed to Trader Joe’s grocery stores in Illi-nois, Indiana, Iowa, Kansas, Kentucky, Michigan, Minnesota, Missouri, Nebraska, Ohio & Wisconsin.
The voluntary recall applies to product in a 6 ounce, plastic container with UPC # 00666695 and a SELL BY Date of JUN 10, 2014, stamped on the edge of the lid.
The potential for contamination was found during a routine testing by the Company. No illnesses have been reported.
Lansal, Inc. has contacted the retailer and distributors instructing them to remove all affected product from sale and is working with the appropriate agencies including state Departments of Health, the Food and Drug Administration and local authorities.
Consumers who have purchased the above product code are urged not to eat it and to dispose of it or return it to the place of purchase for a full refund. Consumers with any questions may call toll free (877) 877-907-7508 from 8:00A.M. to 8:00P.M. Central Daylight Time, 7 days a week.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Wegmans Issues Voluntary Recall of Bakery Products That May Contain Fresh Peaches, Nectarines and Plums Supplied by Wawona Packing Company
Contact:
Consumer:
1-855-934-3663
Media:
Jo Natale
1-585-301-8009
jo.natale@wegmans.com
FOR IMMEDIATE RELEASE - July 20, 2014 - Rochester, NY - Wegmans Food Markets, Inc. is voluntarily recalling several in-store baked desserts that may contain fresh peaches, nectarines, and/or plums. The fruit was supplied by California-based Wawona Packing Company, which issued a voluntary recall when routine testing by the company showed potential contamination with Listeria monocytogenes. No illnesses associated with this recall have been reported to Wawona or to Wegmans.
L. monocytogenes is a bacterium that can contaminate foods and cause a mild non-invasive illness (called listerial gastroenteritis) or a severe, sometimes life-threatening, illness (called invasive listeriosis). Persons who have the greatest risk of experiencing listeriosis after consuming foods contaminated with L. monocytogenes are fetuses and neonates who are infected after the mother is exposed to L. monocytogenes during pregnancy, the elderly, and persons with weakened immune systems. Customers who have experienced these symptoms should contact their physician.
The following recalled products may contain the affected Wawona-packed fruits. The products are labeled with a store-printed scale label that will identify the product and UPC.
Recalled Cakes and Pies
Peach Melba Whipped Cream, 34 oz. UPC 7789033104
Fruit-Topped Short Cake, 1/4 sheet, 49 oz. UPC 7789032772
Genoise Cake,1/4 sheet, 64 oz. UPC 7789027385
Fruit-Topped Cheese Cake, large, 54 oz. UPC 7789026438
Fruit-Topped Cheese Cake, small, 18 oz. UPC 7789026441
Fruit-Topped Cream Cheese Pie 40 oz. UPC 7789018953
Recalled Tarts and Other Pastries
Vanilla Trifle, 8 oz. UPC 7789080600
Peach Melba Tart, 26 oz. UPC 7789098553
Rectangular Fruit Tart, 37 oz. UPC 20823800000
Mixed Fruit Tart, 30 oz. UPC 20819500000
Square Fruit Tart, 48 oz. UPC 20823700000
Lg. Fruit Strip (Puff Pastry), 11 oz. UPC 20829200000
Sm. Fruit Strip (Puff Pastry), 3 oz. UPC 20829100000
Frangipane (tart), 30 oz. UPC 7789091064
Lg. Fruit Crostata, 21 oz. UPC 20829300000
Sm. Fruit Crostata, 7 oz. UPC 20829900000
Lg. Nectarine Crostata, 21 oz. UPC 20823100000
Sm. Nectarine Crostata, 6 oz. UPC 20832600000
Customers who purchased the recalled products from Wegmans between June 1 and July 20 should discard the product at home and visit the service desk and identify the product for a full refund.
Wegmans will place automated phone calls to customers who purchased the recalled products using their Shoppers club card. Consumers with questions may contact Wegmans consumer affairs department toll free at 1-855-934-3663 Monday through Friday, between 8:00 a.m. and 5:00 p.m. Eastern time.
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(CNN) -- If you've picked up fruit at Costco, Trader Joe's, Kroger or Walmart stores recently, keep reading.
Wawona Packing Co. is voluntarily recalling peaches, nectarines, plums and pluots that were packed at its Cutler, California, warehouses between June 1 and July 12. Wawona believes the products may be contaminated with Listeria monocytogenes.
Costco, Trader Joe's, Kroger and the Walmart Corp. -- which operates Walmart and Sam's Club stores, have all posted notices about the fruit recall on their websites. The recall is nationwide, according to the U.S. Food and Drug Administration.
-CNN, read more ... (http://www.cnn.com/2014/07/22/health/costco-fruit-recall/index.html?hpt=hp_t2)
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Wawona Packing Co. Takes Precautionary Step of Voluntarily Recalling Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk
Contact:
Consumer:
1-888-232-9912
Media:
Amy Philpott
703-472-6615
FOR IMMEDIATE RELEASE - July 19, 2014 - Wawona Packing Company of Cutler, Calif is voluntarily recalling certain lots of whole peaches (white and yellow), nectarines (white and yellow), plums and pluots packed between June 1, 2014 through July 12,2014 due to the potential of the products being contaminated with Listeria monocytogenes. Wawona Packing has notified retailers of the specific lots being recalled. No other products are impacted by this recall. No illnesses have been linked to this recall to date.
Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The recalled products were shipped directly to retailers and wholesalers who resell the products. Because we do not know the locations of the companies that purchased the products from our direct customers, the company is issuing a nationwide recall. Consumers can identify the recalled products by the information provided in the attached list and photographs. Anyone who has the recalled products in their possession should not consume them and should discard them. Consumers with questions may contact Wawona Packing at 1-888-232-9912, M-F, 8am-5pm ET , or visit www.wawonapacking.comdisclaimer icon for a copy of this press release.
Wawona Packing has already notified its business customers and requested that they remove the recalled products from commerce. Wawona Packing is voluntarily recalling these products in consultation with the U.S. Food and Drug Administration
The recall was initiated based on internal company testing. The company shut down the implicated packing lines, retrofitted equipment, sanitized the facility and retested. Subsequent daily test results have been negative.
"We are aware of no illnesses related to the consumption of these products" said Brent Smittcamp, President of Wawona Packing Co. " By taking the precautionary step of recalling product, we will minimize even the slightest risk to public health, and that is our priority."
Wawona Packing Recalls Product List - 16 pages of specific lot numbers (http://www.fda.gov/downloads/Safety/Recalls/UCM405955.pdf)
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Wawona Packing Co. Expands Its Voluntary Recall of Fresh, Whole Peaches, Plums, Nectarines, and Pluots Because of Possible Health Risk
Contact
Consumer:
1-888-232-9912
FOR IMMEDIATE RELEASE - July 31, 2014 - Out of an abundance of caution, Wawona Packing Company of Cutler, California is expanding its voluntary recall from July 19, 2014, of whole white and yellow peaches, white and yellow nectarines, plums and pluots due to the potential of the products being contaminated with Listeria monocytogenes.
Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The July 19 recall covered specific lots of products packed from June 1 through July 12, 2014. Wawona Packing Company is expanding the recall, as a precautionary step, to cover all products packed in the Wawona Packing Co. facility from June 1, 2014 through July 17, 2014 because the company’s experts have yet to identify with scientific certainty the source of Listeria monocytogenes in the facility.
Beginning on July 18, 2014, no products have been packed at the Wawona Packing facility in Cutler, CA. Products packed on or after July 18 outside of the Wawona Packing Co. facility are not affected by this recall.
Consumers can identify the recalled products by the information provided in the attached photographs. The recalled products include the following brands marketed to consumers: Sweet 2 Eat, Sweet 2 Eat Organic, Mrs. Smittcamp’s, and are also packed in private labels. These brands will be on the boxes or on the stickers placed on individual fruit. Anyone who has the recalled products in their possession should not consume them and should discard them. If consumers are seeking reimbursement, they should return to the store where they purchased the product to request a refund, providing proof of purchase or receipt if available. Consumers with questions may contact Wawona Packing’s consumer information desk at 1-888-232-9912, M-F, 8am-11pm EST or Sat-Sun 8am-8pm EST, or visit www.wawonapacking.comdisclaimer icon for a copy of this press release and product photos.
Wawona Packing shipped the recalled products directly to retailers and wholesalers who resell or further distribute the products. Because we do not know the locations of the companies or stores that received the products from our direct customers, the company is issuing a nationwide recall.
Wawona Packing has already notified its business customers of the expanded recall, and requested that they remove the additional recalled products from commerce. Wawona Packing is voluntarily recalling these products in consultation with the U.S. Food and Drug Administration.
The July 19 recall was initiated based on internal company testing. The company shut down the packing lines, retrofitted equipment, sanitized the facility, and is working with experts on Listeria in making further improvements to the food safety program. Our packing lines in the Cutler, California facility will not reopen until we know, in consultation with experts, that they are safe.
“Wawona Packing believes in the highest standards of food safety. We have been working around the clock to determine the source of the Listeria monocytogenes. We have brought in nationally known experts in food safety to investigate every part of our packing facility, and we are working with the U.S. Food & Drug Administration,” said company president Brent Smittcamp.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and safety alerts from states as a service to consumers, the media, and other interested parties. FDA is not responsible for the content of these notices.
Henry’s Farm Inc. Recalls Soybean Sprouts Due To Possible Health Risk
Contact:
Consumer:
301-802-2996
FOR IMMEDIATE RELEASE November 24, 2014 - Henry’s Farm Inc. of Woodford, VA is recalling all packages of Soybean Sprouts because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections to individuals with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The following products are being recalled by the firm.
All clear 1 lb packages of Natto Soybean Sprouts. These products are labeled as produced by Henry’s Farm Inc. The packages were not coded.
All clear 2 lb packages of Bean Sprouts. These products are labeled as distributed by Rhee Bros. Inc. Columbia, MD. The packages were not coded.
All bulk (approximately 10 lbs.) black plastic bags of Soy Bean Sprouts. These products are labeled as produced by Henry’s Farm Inc. The packages were not coded.
These items were distributed to retail stores in Virginia and Maryland.
The contamination was discovered after sampling by the Virginia Department of Agriculture and Consumer Services Food Safety & Security Program and subsequent analysis by the Virginia Division of Consolidated Laboratory Services revealed the presence of Listeria monocytogenes in the products. No illness has been reported to date.
Individuals who purchased Soybean Sprouts, distributed by Henry’s Farm should return the product to the place of sale for a full refund.
Consumers with questions may contact the company directly at 301-802-2996 or the Virginia Department of Agriculture and Consumer Services, Food Safety and Security Program at 804-786-3520.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Del Monte Fresh Produce N.A., Inc. Voluntarily Recalls Fresh Cut Fruit Containing Gala Red Apple in a Few States in North East US Because of Possible Health Risk
Contact:
Consumer:
1-800-659-6500
FOR IMMEDIATE RELEASE — December 10, 2014 — CORAL GABLES, Fla — Del Monte Fresh Produce N.A., Inc. (“Del Monte Fresh”) announced today the voluntary recall of fresh cut fruit containing Gala red apples grown in Pennsylvania. The affected product was distributed to a limited number of customers in a few States in North East US and is being recalled because these apples have the potential to be contaminated with Listeria monocytogenes , an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.
Listeriosis symptoms may include fever and muscle aches, sometimes preceded by diarrhea and other gastrointestinal distress, according to the Centers for Disease Control and Prevention. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among women who are pregnant.
A total of 3,051 consumer packages containing fresh cut red apples were distributed to Giant Eagle, Amazon Fresh, Sunoco, Peter’s Fruit, Wegmans, Sheetz and 7-Eleven and have “Best If Enjoyed By” dates of 12/3/14, 12/6/14, 12/7/14 and 12/8/14. The fresh cut red apples have a red color skin. The recalled fresh cut fruit packages containing red apples were distributed for sale in clear plastic containers with one of the following labels and markings:
Click on link for list: http://www.fda.gov/Safety/Recalls/ucm426419.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery
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Caramel apples linked to fatal listeria outbreak
By Jen Christensen, CNN
updated 5:57 PM EST, Fri December 19, 2014
(CNN) -- A sweet treat has turned potentially deadly for dozens of people in multiple states.
At least four people have died -- in a fifth case tests are pending -- after eating caramel apples that may have been infected with Listeria monocytogenes.
Some 28 people have become infected with the deadly bacterium in 10 different states according to the Centers for Disease Control and Prevention.
Listeria What you need to know
Of the people who have gotten sick, nine were pregnant. Pregnant women are 10 times more likely to get listeriosis after eating infected food.
More here: http://www.cnn.com/2014/12/19/health/caramel-apple-listeria/index.html?hpt=hp_inthenews
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Kkot Saem Sprouts, Inc. Recalls Soybean Sprouts and Mungbean Sprouts Because of Possible Health Risk
Contact:
Consumer:
253-226-7569
FOR IMMEDIATE RELEASE – December 19, 2014 – Kkot Saem Sprouts, Inc. of Spanaway, Washington is voluntarily recalling Soybean Sprouts and Mungbean Sprouts sold under brand names Kkot Saem, Winter Blossom Bean Sprouts, and Winter Blossom because it has the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
Soybean Sprouts and Mungbean Sprouts were distributed at H-Mart in Washington and Oregon, and G-Mart in Oregon and the last date of distribution was on December 16, 2014. The mungbean sprouts product has a 5-day shelf life from the packing date and soybean sprouts product has a shelf life of up to two weeks from the packing date.
RECALLED PRODUCT Brand NET WT. PACKAGE TYPE UPC
Soybean Sprouts Winter Blossom Bean Sprouts 1.5 lbs. Plastic bag, multi-colored with orange stripe on top, lower middle portion and at bottom. Orange & black English and Korean letters on white background on front of bag. 0 94922 55330 0
Soybean Sprouts un-labeled 5 lbs. Clear plastic bag with no label None
Mungbean Sprouts Kkot Saem Winter Blossom Bean Sprouts 0.8 lb Clear plastic bag with blue letters on white background. English and Korean letters on front of bag. 1 80036 83737 2
Mungbean Sprouts Kkot Saem 2 lbs. Clear plastic bag with no label 0 94922 55334 8
Mungbean Sprouts Kkot Saem 5 lbs. Clear plastic bag with no label None
Mungbean Sprouts Winter Blossom Bean Sprouts 10 lbs. Orange and blue labeling in Korean and English on white background. 0 94922 55331 7
This recall was the result of the sample collected and analyzed by the Food and Drug Administration and it is revealed that the finished mungbean sprouts contained Listeria monocytogenes.
There have been no illnesses or deaths reported to date. This recall is being made with the knowledge of the U.S. Food and Drug Administration.
Consumers who have purchased these recalled products are urged to return them to the place of purchase or discard products. Consumers who have questions should call Kkot Saem Sprouts, Inc. at 253-226-7569, Monday - Friday, 8 am - 5 pm PST.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Press Release for Hanbit Enterprises, Inc. dba Jack and the Beanstalk Recalls Soybean Sprouts Because of Possible Health Risk
Contact:
Consumer:
831-422-8028
FOR IMMEDIATE RELEASE — February 13, 2015 — Hanbit Enterprises, Inc. dba Jack and the Beanstalk is recalling Soybean Sprouts in 1lb, 1.5lb, 10 lb, and Natto plastic bags distributed up to and including February 12, 2015 with Best if Used by dates up to February 19, 2015, because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer long-‐term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The soybean sprouts were distributed to Bay Area stores and restaurants.
1LB SOYBEAN SPROUT BAR CODE – 7-27580-12366-9
1.5LB SOYBEAN SPROUT BAR CODE – 7-27580-12365-2
10LB SOYBEAN SPROUT BAR CODE – 7-27580-12351-5
NATTO SOYBEAN SPROUT BAR CODE – 7-27580-12367-6
No illnesses that have been reported to date.
The recall was the result of a routine sampling program by the FDA which revealed that the finished products contained the Listeria bacteria. The company has ceased the production and distribution of the product as FDA and the company continues their investigation as to what caused the problem.
Consumers who have purchased Hanbit Enterprises, Inc. soybean sprouts in 1lb, 1.5lb, 10lb, and Natto plastic bags are urged to return it to the place of purchase for a full refund.
Consumers with questions may contact the company at 831-422-8028 during office hours: Monday through Friday from 9 a.m. to 5:00 p.m.
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We assume this is the San Francisco Bay Area since the bean sprouts appear to have come from Salinas Cal.
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Tainted dairy investigation.
Recall -- Firm Press Release
The information in this posting reflects the FDA’s best efforts to communicate what it has learned from the manufacturer, the CDC, and the state and local public health agencies involved in the investigation. The agency will update this page as more information becomes available.
Product Removal/Foodborne Illness Outbreak Investigation Advisory
The U.S. Food and Drug Administration along with the Centers for Disease Control and Prevention (CDC) and state and local officials are investigating an outbreak of listeriosis potentially linked to certain Blue Bell Creameries single serving ice cream products. Listeriosis is caused by the bacterium Listeria monocytogenes.
Story - Tainted Blue Bell Ice Cream causing Hospitalizations (http://www.fda.gov/Safety/Recalls/ucm438626.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery)
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Wegmans Announces Recall of (Frozen) Wegmans Organic Food You Feel Good About Just Picked Spinach, 12 Oz. Which May Be Contaminated With Listeria Monocytogenes
Contact:
Consumer:
1-855-934-3663
Media:
585-429-3627 or 585-301-8009
FOR IMMEDIATE RELEASE — March 23, 2015 — ROCHESTER, NY — Wegmans Food Markets, Inc. is recalling approximately 12,540 packages of Wegmans Organic Food You Feel Good About Just Picked Frozen Spinach, 12 oz. (UPC 77890-32932) due to possible contamination with Listeria monocytogenes. The product was sold in the frozen food department of the company’s 85 stores in New York, Pennsylvania, New Jersey, Virginia, Maryland, and Massachusetts between January 27 and March 21, 2015. Only packages with the following codes are affected:
BEST USED BY JAN 26 2017 50265
BEST USED BY FEB 02 2017 50335
This product is supplied to Wegmans by Twin City Foods, Inc. based in Stanwood, Washington.
L. monocytogenes is a bacterium that can contaminate foods and cause a mild non-invasive illness (called listerial gastroenteritis) or a severe, sometimes life-threatening, illness (called invasive listeriosis). Persons who have the greatest risk of experiencing listeriosis after consuming foods contaminated with L. monocytogenes are fetuses and neonates who are infected after the mother is exposed to L. monocytogenes during pregnancy, the elderly, and persons with weakened immune systems. Customers who have experienced these symptoms and are concerned should contact their physician.
No illnesses associated with this recall have been reported to date.
Wegmans will place automated phone calls to customers who purchased the product using their Shoppers Club card. Customers who purchased the recalled products from Wegmans should return it to the service desk for a full refund.
Consumers with questions may contact Wegmans consumer affairs department toll free at 1-855-934-3663 Monday through Friday, between 8:00 a.m. and 5:00 p.m. Eastern time.
###
Wegmans Food Markets, Inc. is an 85-store supermarket chain with stores in New York, Pennsylvania, New Jersey, Virginia, Maryland, and Massachusetts. The family-owned company, founded in 1916, is recognized as an industry leader and innovator.
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More tainted spinach:
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Amy’s Kitchen Recalls Various Products Because of Possible Health Risk
Contact:
Consumer:
707-781-7535
FOR IMMEDIATE RELEASE – March 22, 2015 – Petaluma, California – Amy’s Kitchen, Inc. is voluntarily recalling approximately 73,897 cases of select code dates and manufacturing codes of the products identified on Attachment A. This recall is based on a recall notice from one of Amy’s organic spinach suppliers that Amy’s may have received organic spinach with the possible presence of Listeria monocytogenes, an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Amy’s Kitchen is not aware of any illness complaints to date related to the recalled products identified in Attachment A. Out of an abundance of caution, however, Amy’s Kitchen is recalling these products based on the recall notice we received from our supplier.
The recalled products were distributed to stores nationwide in the United States and in Canada.
The recalled products are identified in Attachment A, and no other products or varieties are included in this recall.
Amy’s Kitchen has notified its distributors and retailers and is taking this voluntary action as a precautionary measure. This recall is being conducted with the knowledge of the Food and Drug Administration.
Consumers who have any of the products identified in the chart above are urged to dispose them or return them to the store where they were purchased for an exchange or full refund. Consumers may also call Amy’s at (707) 781-7535 [Monday through Friday between 9 a.m. and 5 p.m. (Pacific)].
Extensive List of affected products (http://www.fda.gov/Safety/Recalls/ucm439397.htm?source=govdelivery&utm_medium=email&utm_source=govdelivery)
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
La Terra Fina Recalls Organic Spinach Dip Sold in Bay Area Costco Clubs
Contact:
Consumer:
510-999-0050
FOR IMMEDIATE RELEASE — March 20, 2015 — UNION CITY, CA, La Terra Fina is issuing a voluntary recall of its Organic Spinach Dip due to a potential health risk from Listeria exposure. The recall of product available in Bay Area Costco stores is a precaution. This is the only product that has been impacted and there have been no reports of illness.
Product Name
La Terra Fina Organic Thick &
Creamy Spinach Dip & Spread,
24-ounce tub
UPC Code
640410513730
Best-By Date
3/24/2015
4/01/2015
4/14/2015
4/20/2015
The quality of its products and satisfaction of its customers is La Terra Fina’s top priority. The brand follows rigorous food safety and ingredient testing standards and is withdrawing this product out of an abundance of caution for consumer safety. La Terra Fina urges consumers who have purchased this item in the impacted region to discard any opened or unused product and contact their local Costco store for a refund.
Consumer questions on the issue can be directed to La Terra Fina’s Consumer Affairs by calling 510-999-0050.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Twin City Foods, Inc. Recalls Frozen Cadia Organic Cut Spinach, Meijer Organics Chopped Spinach, Wild Harvest Organic Cut Leaf Spinach, and Wegmans Organic Just Picked Spinach Because of Possible Health Risk
Contact:
Consumer:
(804) 385-3772
FOR IMMEDIATE RELEASE — March 24, 2015 — Twin City Foods, Inc. of Stanwood, Washington is recalling the following products because they have the potential to be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, listeria infection can cause miscarriages and stillbirths among pregnant women.
Cadia Organic Cut Spinach, 16 oz. frozen packages
UPC 15369 01165
Package code: 23424
Product distributed only in California
Meijer Organics Chopped Spinach, 16 oz. frozen packages
UPC 41250 02362
Package code: BEST BY FEB 2017 50415
Distributed to warehouses in MI, OH, and WI
Wild Harvest Organic Cut Leaf Spinach, 16 oz. frozen packages
UPC 11535 50170
Package code: SELL BY 08.DEC.2016 L084WE, Distributed to warehouses in AZ, CA, WA
Package code: SELL BY 22.JAN.2017 A225WE, Distributed to warehouses in PA and VA
Package code: SELL BY 30.JAN.2017 A305WE, Distributed to warehouses in DE, ME, PA, and VA
Package code: SELL BY 04.MAR.2017 C045WE, Distributed to warehouses in ME and PA
Wegmans Organic Just Picked Spinach, 12 oz. frozen packages
UPC 77890 32932
Package code: BEST USED BY JAN.26.2017 50265, Distributed to warehouses in NY and PA
Package code: BEST USED BY FEB.02.2017 50335, Distributed to warehouses in NY and PA
No illnesses have been reported to date.
The Recalled Product was supplied to Twin City Foods by Coastal Green Vegetable Company LLC of Oxnard, CA which initiated a recall of the bulk spinach on March 20, 2015 due to possible contamination with Listeria monocytogenes. Twin City Foods immediately notified all affected customers and initiated recalls of the retail packages on March 20, 2015.
Consumers who have purchased the affected product are urged to not consume the product and immediately return the product to the store where they purchased it for a full refund. Consumers with questions may contact the retailer at which they purchased the affected product.
This recall is being made with the knowledge of the U.S. Food and Drug Administration.
Consumers with any questions may contact Mark Hubbard at (804) 385-3772 Monday through Friday, between 8:00 a.m. and 5:00 p.m. Eastern time, or email to mhubbard@mwcllc.com.
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Superior Foods, Inc., of Watsonville, CA is recalling 8,475 Cases Of Simply Balanced 10-oz Frozen Organic Chopped Spinach Distributed Exclusively At Target Stores.
Contact:
Consumer:
1-866-672-0811
FOR IMMEDIATE RELEASE — March 24, 2015 — Watsonville, CA — This recall is based on a recall notice from one of Superior Foods, Inc., organic frozen spinach suppliers that Superior Foods, Inc., may have received organic spinach with the possible presence of Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
Product was distributed Nationwide at Target retail stores.
Simply Balanced Organic Chopped Spinach 10-oz steam in bag
DPCI # (Department, Class, Item.) 270-00-0663
UPC Code - 85239 00663
Production Date Code and Best By Code
4360SF3 through 7 J1 Best By 26/06/2016
4360SF3 through 7 J2 Best By 26/06/2016
5026SF4 through 8 J1 Best By 26/07/2016
5026SF4 through 8 J2 Best By 26/07/2016
5051SF2 through 4 J1 Best By 20/08/2016
5051SF2 through 4 J2 Best By 20/08/2016
Superior Foods Inc., is not aware of any illness complaints to date related to this event. Out of an abundance of caution, however, Superior Foods, Inc., is recalling these products based on the recall notice we received from our supplier. This recall is being conducted with the knowledge of the Food and Drug Administration.
Consumers who have any of the product identified are urged to dispose it, or return it to the store where it was purchased for an exchange or full refund.
Consumers with questions may call 1-866-672-0811 Monday through Friday between 8 a.m. and 5 p.m. Eastern Standard Time.
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The organic spinach recall is widening on this product.
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
La Terra Fina Recalls Various Products Due to Supplier Recall of Organic Spinach
Contact:
Consumer:
510-404-5889
Media:
Nicole Dionisopoulos, Maxwell PR
(503) 231-3086 / nicole@maxwellpr.com
FOR IMMEDIATE RELEASE – March 24, 2015 – Union City, CA – Due to receiving a recall notice from its organic spinach supplier because of possible Listeria monocytogenes exposure, La Terra Fina is recalling the products outlined in the chart below. Following its voluntary recall of Organic Spinach Dip last Friday, La Terra Fina is expanding the recall to include these products that were manufactured on the same production equipment on the same day as the Organic Spinach Dip and are being recalled out of an abundance of caution.
Listeria monocytogenes is an organism that can cause infections in young children, frail or elderly people, and others with weakened immune systems. The recalled products were distributed to Costco stores in the Northwest, Midwest, Northeast and Southeast regions and Smart & Final stores along the West Coast only.
To-date, there have been no confirmed cases of illness in relation to these products. The FDA is aware that the company is undertaking this voluntary action, which is out of an abundance of caution for consumers' well-being and safety.
Only products with the following "best by" dates are being recalled. The "best by" date for each product can be found on the side of the container. Consumers who have purchased these products are urged to discard or return the place of purchase for a full refund. For more information consumers can call La Terra Fina at 510-404-5889 between Monday and Friday, 8:30AM - 5PM US PST.
Recalled Products
Product Description Item # UPC Code Best By Date Retailer Region
Spinach Artichoke & Parmesan Dip made with Greek Yogurt 31oz. tub 379903 6-40410-51338-9 4/14/15
4/20/15 Costco - NW Region
Chunky Spinach Artichoke & Parmesan Dip 31oz. tub 407600 6-40410-51193-4 3/31/15
4/5/15
4/29/15 Costco - MW, NE & SE Regions
Chunky Spinach Artichoke & Parmesan Dip 31oz. tub 4300193 6-40410-51193-4 3/28/15
4/29/15 Smart & Final-West Coast
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Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
Henry’s Farm Inc. Recalls Soybean Sprouts Due To Possible Health Risk
Contact:
Consumer:
301-802-2996 or 804-786-3520
FOR IMMEDIATE RELEASE — April 3, 2015 — LOCATION — Henry’s Farm Inc. of Woodford, VA is recalling all packages of soybean sprouts because they may be contaminated with Listeria monocytogenes, an organism which can cause serious and sometimes fatal infections to individuals with weakened immune systems. Although healthy individuals may suffer only short term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.
The following products are being recalled by the firm.
1-lb bags of soybean sprouts in clear plastic bags labeled “Natto Soybean Sprouts” “Keep Refrigerated” with a UPC Code of 1303020000 produced on or after March 24, 2015.
10-lb bags of soybean sprouts in black plastic bags labeled “Soy Bean Sprouts” “Keep Refrigerated” produced on or after March 24, 2015.
These items were distributed to retail stores in Virginia and Maryland.
The contamination was discovered after sampling by the Virginia Department of Agriculture and Consumer Services Food Safety Program and subsequent analysis by the Virginia Division of Consolidated Laboratory Services revealed the presence of Listeria monocytogenes in the products. No illness has been reported to date.
Individuals who purchased soybean sprouts, distributed by Henry’s Farm should return the product to the place of sale for a full refund.
Consumers with questions may contact the company directly at 301-802-2996 or the Virginia Department of Agriculture and Consumer Services, Food Safety Program at 804-786-3520.
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Here is another spinach recall:
Recall -- Firm Press Release
FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company.
La Terra Fina Expands Voluntary Product Recall to Include a Single Lot of Its 10-Ounce Chunky Spinach Artichoke & Parmesan Dip & Spread, Due to Supplier Recall of Organic Spinach
Contact:
Consumer:
877-929-2575
Media:
Nicole Dionisopoulos, Maxwell PR
(503) 231-3086 / nicole@maxwellpr.com
FOR IMMEDIATE RELEASE — March 31, 2015 — UNION CITY, Calif. — Due to receiving a recall notice from its organic spinach supplier because of possible Listeria monocytogenes exposure, La Terra Fina is expanding its voluntarily recall to include one lot of its 10-ounce Chunky Spinach Artichoke & Parmesan Dip & Spread as outlined in the chart below. This action is being taken out of an abundance of caution due to this product having been manufactured on the same production equipment on the same day as the Organic Spinach Dip.
Listeria monocytogenes is an organism that can cause infections in young children, frail or elderly people, and others with weakened immune systems. The recalled products were distributed in select retailers in the Midwest, West Coast and Rocky Mountain regions.
To date, there have been no confirmed cases of illness in relation to these products. The FDA is aware that the company is undertaking this voluntary action, which is out of an abundance of caution for consumers’ well-being and safety.
Only 10 oz. products with the "best by" date below are being recalled. The "best by" date for each product can be found on the side of the container. Consumers who have purchased these products are urged to discard or return to the place of purchase for a full refund. For more information, consumers can call the La Terra Fina Consumer Affairs Call Center at 877-929-2575 between Monday and Friday from 8:00AM - 8:00PM US EDT.
Recalled Product
Product Description UPC Code
10-ounce Chunky Spinach Artichoke & Parmesan Dip & Spread 6-40410-51327-3
Best By Date Retailer Region
4/5/15 Midwest, West Coast & Rocky Mountain regions
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