Summary
The FDA issued a Class II for TILAPIA FILLET 5-7 OZ BLSL, TUNA LOIN AHI 3-5LB by Ben E Keith Foods - Fort Worth. Reason: A frozen/ refrigerated food trailer holding various types and brands of frozen/ refrigerated foods were temperature abused..
Details
Source
Food Recall
External ID
F-0570-2024
Action Date
2023-12-20
Status
Terminated
Category
food
Product Description
TILAPIA FILLET 5-7 OZ BLSL, TUNA LOIN AHI 3-5LB
Lot/Code Info: unknown
Quantity Affected: 1721 cases total of various products
Reason for Recall
A frozen/ refrigerated food trailer holding various types and brands of frozen/ refrigerated foods were temperature abused.
Distribution
All products were shipped via truck to food services.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-10-12
Company
Fort Worth, TX
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 143 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Ben E Keith Foods - Fort Worth has 8 FDA actions in our database, including 8 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 (Ben E Keith Foods - Fort Worth) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ben E Keith Foods - Fort Worth have FDA actions?
Ben E Keith Foods - Fort Worth has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0570-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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