ZIP International Group, LLC Expands Alert on Listeria in Sliced Herring Fillet in oil (forelka) 330 gram and 600 gram

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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.

 

ZIP International Group, LLC Expands Alert on Listeria in Sliced Herring Fillet in oil (forelka) 330 gram and 600 gram

 

Contact:
Consumers:
Zip International Group LLC
732-225-3600

FOR IMMEDIATE RELEASE - February 9, 2012 -ZIP INTERNATIONAL GROUP LLC, 160 Raritan Center Parkway #6, Edison, NJ  08837 is expanding its recall of sliced herring fillet (forelka) 330 gram and 600 gram in plastic packaging due  to Listeria contamination. 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 sliced herring fillet (forelka) 330 gram and 600 gram in plastic packaging includes best by date 5/18/2012 . The best by date is located on the round side of the packaging and was sold to retail grocery stores in New York State. It is a product of Ukraine.

The recall was initiated after routine sampling by New York State Department of Agriculture & Markets Food Inspectors and subsequent analysis of the product by Food Laboratory personnel found the product to be positive for Listeria monocytogenes.

No illnesses have been reported to date in connection with this problem. Consumers who have purchased sliced herring fillet (forelka) should not consume it, but should return it to the place of purchase. Consumers with questions may contact the company @ 732-225-3600, 9:00AM-5:00 PM EST from Monday to Friday.

 

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Original Press Release dated January 10, 2012

    

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Read more http://www.fda.gov/Safety/Recalls/ucm291347.htm

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