RecallHawk
Class II Recall

AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, net wt. 5 lbs. UPC 731149654075. Product was sold at WinCo.

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Summary

The FDA issued a Class II for AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, net wt. 5 lbs. UPC 731149654075. by Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.. Reason: Shrimp may be contaminated with Cesium-137 (Cs-137)..

Details

Source

Food Recall

External ID

H-0162-2026

Action Date

2025-11-12

Status

Ongoing

Category

food

Product Description

AquaStar 16/20 Frozen Raw EZ-Peel White Shrimp, net wt. 5 lbs. UPC 731149654075. Product was sold at WinCo.

Lot/Code Info: 10662 5117 10 10/27/2027 10662 5118 09 10/28/2027 10662 5118 10 10/28/2027 10662 5119 09 10/29/2027 10662 5120 09 10/30 /2027 10662 5122 10 11/02/2027 10662 5122 11 11/02/2027 10662 5123 10 11/03/2027

Quantity Affected: Total 7200 cases (4/5lbs. bags per case)

Reason for Recall

Shrimp may be contaminated with Cesium-137 (Cs-137).

Distribution

Nationwide.

Type: Voluntary: Firm initiated

Recall Initiated: 2025-09-20

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 34 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. has 12 FDA actions in our database, including 12 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 (Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. have FDA actions?

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. has 12 FDA actions in our database, including 12 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "H-0162-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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