RecallHawk
Class II Recall

AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs. UPC 731149390010. Product is packaged in a printed bag with

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Summary

The FDA issued a Class II for AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs. UPC 731149390010. P 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-0159-2026

Action Date

2025-11-12

Status

Ongoing

Category

food

Product Description

AquaStar Raw Peeled Tail-on Shrimp Skewers, net wt. 1.25lbs. UPC 731149390010. Product is packaged in a printed bag with a black top and blue bottom and printed pictures of the skewers inside.

Lot/Code Info: Lot code 10662 5127 10, Best If Used By: 11 07 2027 Lot code 10662 5128 11, Best If Used By: 11 08 2027 Lot code 10662 5133 11, Best If Used By: 11 13 2027 Lot code 10662 5135 10, Best If Used By: 11 15 2027

Quantity Affected: 5220 cases (8/1.25lbs. bags)

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-0159-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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