RecallHawk
Class III Recall

UPC 23308200000 TILAPIA TORTILLA CRUSTED This is Albertson's store-made item and sold by random we

Albertsons Companies LLC

Summary

The FDA issued a Class III for UPC 23308200000 TILAPIA TORTILLA CRUSTED This is Albertson by Albertsons Companies LLC. Reason: Contains statement does not declare Tilapia.

Details

Source

Food Recall

External ID

H-1040-2026

Action Date

2026-06-10

Status

Ongoing

Category

food

Product Description

UPC 23308200000 TILAPIA TORTILLA CRUSTED This is Albertson's store-made item and sold by random weight at point of sale with grocery store's scale label.

Lot/Code Info: Product was labeled with a Packed On date of May 05. 26 or before.

Quantity Affected: 208 units

Reason for Recall

Contains statement does not declare Tilapia

Distribution

Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2026-05-06

Company

Context & Analysis

This is a Class III recall. Class III recalls involve products unlikely to cause adverse health consequences, but that violate FDA regulations.

This was one of 166 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls.

Frequently Asked Questions

What is a Class III recall?

A Class III recall involves products that are unlikely to cause adverse health effects but violate FDA labeling or manufacturing regulations.

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 (Albertsons Companies LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Albertsons Companies LLC have FDA actions?

Albertsons Companies LLC has 174 FDA actions in our database, including 174 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-1040-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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