AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs. UPC 731149654051. Product was sold at Publix.
Summary
The FDA issued a Class II for AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs. UPC 731149654051. 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-0163-2026
Action Date
2025-11-12
Status
Ongoing
Category
food
Product Description
AquaStar 13/15 Raw Shrimp Easy Peel Deveined, net wt. 2 lbs. UPC 731149654051. Product was sold at Publix.
Lot/Code Info: 10662 5115 11 Oct 25 2027 10662 5116 10 Oct 26 2027
Quantity Affected: 1800 cases (10/2lbs. Pkgs. 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
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 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-0163-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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