Premo Meat Lovers 7oz, clear plastic, UPC 612510093832, 4 retail packages per wholesale case
Summary
The FDA issued a Class II for Premo Meat Lovers 7oz, clear plastic, UPC 612510093832, 4 retail packages per by Lipari Foods Operating Company, LLC.. Reason: Potential contamination with Salmonella.
Details
Source
Food Recall
External ID
F-1649-2024
Action Date
2024-08-14
Status
Terminated
Category
food
Product Description
Premo Meat Lovers 7oz, clear plastic, UPC 612510093832, 4 retail packages per wholesale case
Lot/Code Info: Best By Date 7/13/24, Lot Code 25202406
Quantity Affected: 638 cases
Reason for Recall
Potential contamination with Salmonella
Distribution
IL, IN, OH, PA, MI, MD, WV, AR, WI, AL, VA, FL, MO, NY, KY, TN
Type: Voluntary: Firm initiated
Recall Initiated: 2024-06-27
Company
Warren, MI
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 200 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Lipari Foods Operating Company, LLC.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lipari Foods Operating Company, LLC. have FDA actions?
Lipari Foods Operating Company, LLC. has 9 FDA actions in our database, including 9 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1649-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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