• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Safety

  • Print
  • Share
  • E-mail

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.

 

D & M Smoked Fish, Inc. Issues an Allert on Uneviscerated Schmaltz Herring

 

Contact:
(718)523-8899

 

FOR IMMEDIATE RELEASE - July 15, 2010 - D & M Smoked Fish, Inc. located in Queens, New York, is recalling Haifa brand vacuum packaged Schmaltz Herring with the lot number 168, because the product was found to be uneviscerated.

The lot being recalled is a product of Norway, individually vacuum-packed in clear plastic pouches with lot # 168 & Sell by date of 7/20/10 indicated on the label and distributed through food retailers in the NY area.

The Schmaltz Herring was sampled by a New York State Agriculture and Markets Food Inspector during a routine inspection. Analysis of the product by New York State Food Laboratory personnel confirmed that Schmaltz Herring was improperly eviscerated prior to processing.

The sale of uneviscerated fish is prohibited under New York State Agriculture and Markets regulations because of Clostridium Botulinum spores are more likely to be concentrated in the viscera than any other portion of the fish. Uneviscerated fish has been linked to outbreaks of botulism poisoning.

Botulism is a serious and potentially fatal form of food poisoning, causes the following symptoms: general weakness, dizziness, double-vision and trouble with speaking or swallowing.

No illnesses have been reported to date in connection with this problem.

Consumers are warned not to use the product even if it does not look or smell spoiled and should return it to place of purchase. Consumers with questions may contact the company at 718-523-8899.

 

 

###

 

Photo: Product Labels

RSS Feed for FDA Recalls Information [what's this?]