Item Number: 395203 Item Description: TUB LG SUNFLOWER MEAT RAW Case Pack: 12 Package Size: 14 OZ 2-Piece Clear Plastic Tub (No label on Top, Nutritional Label on Bottom) UPC Number: 094776081738

Class I - Dangerous
Recalled: June 4, 2013 Lipari Foods Meat & Poultry

What Should You Do?

  1. Check if you have this product:
    Lot Numbers: 09201304, 24201304, 01201305, 20201305, 30201305 Best By Dates: 4/9/2014, 4/24/2014, 5/1/2014, 5/20/2014, 5/30/2014
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Lipari Foods, Inc.
Reason for Recall:
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 stillbirt
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

Item Number: 395203 Item Description: TUB LG SUNFLOWER MEAT RAW Case Pack: 12 Package Size: 14 OZ 2-Piece Clear Plastic Tub (No label on Top, Nutritional Label on Bottom) UPC Number: 094776081738

Product Codes/Lot Numbers:

Lot Numbers: 09201304, 24201304, 01201305, 20201305, 30201305 Best By Dates: 4/9/2014, 4/24/2014, 5/1/2014, 5/20/2014, 5/30/2014

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: F-1704-2013

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