Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700282 Best Yet Frozen
Summary
The FDA issued a Class II for Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 lbs/pkg; 10 pkgs per 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-0160-2026
Action Date
2025-11-12
Status
Ongoing
Category
food
Product Description
Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700282 Best Yet Frozen Raw EZ-Peel White Shrimp 21/25 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700286 Best Yet Frozen Raw EZ-Peel White Shrimp 26/30 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700283 Best Yet Frozen Raw EZ-Peel White Shrimp 31/40 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700287 Best Yet Frozen Raw EZ-Peel White Shrimp 41/50 (net wt. 1 lbs/pkg; 10 pkgs per case). UPC 04218700284 Best Yet Frozen Raw EZ-Peel White Shrimp 51/60 (net wt. 1 lbs/pkg; 10 pkgs per case).UPC 04218700288 Best Yet brand product was distributed by C&S Wholesale.
Lot/Code Info: Lot code 10662 5111 10 6336 - Best Before 04 21 2027 Lot code 10662 5112 09 6336 - Best Before 04 22 2027 Lot code 10662 5113 10 6336 - Best Before 04 23 2027 Lot code 10662 5114 09 6336 - Best Before 04 24 2027 Lot code 10662 5114 11 6336 - Best Before 04 24 2027 Lot code 10662 5115 10 6336 - Best Before 04 25 2027
Quantity Affected: Total 9900 cases (10/1lb. pkg 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-0160-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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