Listeria bacteria - another recall

[Mimi]

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.

[Mimi]

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).

[Mimi]

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.

[Mimi]

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.

[Mimi]

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.

[Mimi]

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.

[Mimi]

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.

[Mimi]

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.

[Mimi]

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.

[Mimi]

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.

[Mimi]

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

[Mimi]

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.

[Mimi]

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.
 

[Mimi]

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

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

[Mimi]

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.

[Mimi]

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.

[Mimi]

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

[Mimi]

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

[Mimi]

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.

[Mimi]

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.