RecallHawk
Class II Recall

TILAPIA FILLET 5-7 OZ BLSL, TUNA LOIN AHI 3-5LB

Ben E Keith Foods - Fort Worth

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

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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