Item Number: 368768 Item Description: TUB LG SUNFLOWER MEAT R/NS Case Pack: 12 Package Size: 14…
Recalling firm: Lipari Foods, Inc.
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…
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Oct 17, 2013.
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094776081752FDA code information
Lot Numbers: 09201304, 24201304, 20201305, 30201305 Best By Dates: 4/9/2014, 04/24/2014, 05/20/2014, 05/30/2014
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Full FDA record and distribution details
Original product description
Item Number: 368768 Item Description: TUB LG SUNFLOWER MEAT R/NS Case Pack: 12 Package Size: 14 OZ 2-Piece Clear Plastic Tub (No Label on Top, Nutritional Label on Bottom) UPC Number: 094776081752
Extracted codes and context
| Type | Code / value | Context |
|---|---|---|
| UPC | 094776081752 | e Clear Plastic Tub (No Label on Top, Nutritional Label on Bottom) UPC Number: 094776081752 |
| lot | 09201304 | Lot Numbers: 09201304, 24201304, 20201305, 30201305 Best By Dates: 4/9/2014, 04/24/2014, 05/20/2014, 05/30/2014 |
| lot | 20201305 | Lot Numbers: 09201304, 24201304, 20201305, 30201305 Best By Dates: 4/9/2014, 04/24/2014, 05/20/2014, 05/30/2014 |
| lot | 24201304 | Lot Numbers: 09201304, 24201304, 20201305, 30201305 Best By Dates: 4/9/2014, 04/24/2014, 05/20/2014, 05/30/2014 |
| lot | 30201305 | Lot Numbers: 09201304, 24201304, 20201305, 30201305 Best By Dates: 4/9/2014, 04/24/2014, 05/20/2014, 05/30/2014 |
Original FDA recall reason
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
Recall details
- Recall number
- F-1698-2013
- Event ID
- 65392
- FDA status
- Terminated
- Initiated
- Jun 4, 2013
- Reported
- Jul 17, 2013
- Classified
- Jul 11, 2013
- Terminated
- Oct 17, 2013
- Quantity
- 462 cases
- Location
- Warren, MI, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Where it was distributed
Ohio, Michigan, West Virginia, Kentucky, Tennessee, Pennsylvania, Wisconsin, Illinois, and Indiana.
Data updated September 16, 2026. View official FDA data ↗
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