Best Yet Frozen Raw EZ-Peel White Shrimp 16/20 (net wt. 1 lbs/pkg; 10 pkgs per case).
Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. recalled this product and the FDA reported the enforcement action on 12 November 2025 as Class II. The recall was initiated by the firm. Shrimp may be contaminated with Cesium-137 (Cs-137).
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
Product
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.
UPC
04218700282
Reason for recall
Shrimp may be contaminated with Cesium-137 (Cs-137).
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
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
This is one of 9 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 9 separate recalls, which almost every published figure does, overstates it by a factor of 9. All 9 of them are listed on this page.
This recall has no termination date on the record, so as published it had not been terminated under 21 CFR 7.55.
The FDA published the enforcement report 8 weeks after the firm began the recall.
Fish and fishery products are the one food category with their own HACCP regulation in the United States, 21 CFR part 123, because the hazards are species-specific: histamine in scombroid fish, ciguatera in reef fish, and Listeria in cold-smoked products.
Filed under fish and seafood. A product can sit in more than one.
Every product in this recall
The FDA opened 9 enforcement records for this one recall, one per product code. This page carries all of them; the 8 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.
Shrimp may be contaminated with Cesium-137 (Cs-137).
Class II
Other fish and seafood recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Undeclared Soy. Finished product ingredients statement declares Worcestershire sauce but does not declare sub-ingredients Soy Flavoring and Soy Lecithin.
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Recall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.
