RecallHawk
Class I Recall

Ready Meals Crab & Shrimp w/Ccktl SCE NET WT 12 OZ CAL 310 NET WT. 0lb 12oz (340g) ready2eat UPC 23253500000 Store Ba

Albertsons Companies LLC

Summary

The FDA issued a Class I for Ready Meals Crab & Shrimp w/Ccktl SCE NET WT 12 OZ CAL 310 NET WT. 0lb 12oz (3 by Albertsons Companies LLC. Reason: Undeclared allergens; fish, shellfish, egg, wheat, and soy.

Details

Source

Food Recall

External ID

F-1558-2022

Action Date

2022-08-24

Status

Terminated

Category

food

Product Description

Ready Meals Crab & Shrimp w/Ccktl SCE NET WT 12 OZ CAL 310 NET WT. 0lb 12oz (340g) ready2eat UPC 23253500000 Store Banners: ACME, Albertsons, Andronico s Community Markets, Balducci s, Carrs-Safeway, Eagle, Jewel-Osco, King s, Pak N Save, Safeway, Shaw s, Star Market, Vons

Lot/Code Info: All sell thru dates up to and including July 18

Reason for Recall

Undeclared allergens; fish, shellfish, egg, wheat, and soy

Distribution

U.S. distribution to the following: AK, CA, CO, CT, DE, ID, IL, IA, ME, MD, MA, NE, NH, NV, NJ, NM, NY, PA, RI, SD, VT, VA, WA, DC, WY No foreign distribution.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-07-13

Company

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 38 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 I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 "F-1558-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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