← FDA ENFORCEMENT
H-0583-2025Class II

Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.

Recalling firm
Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.
Product type
Food / supplement / cosmetic
Status
Ongoing
Report date
2025-09-24
Distribution
The affected AquaStar brand Cocktail Shrimp, 4oz. shrimp/2oz. cocktail sauce (net wt. 6oz), was sold at WALMART stores in AK, AL, AR, CO, GA, IA, ID, IL, IN, KS, KY, LA, MI, MN, MO, MS, MT, ND, NE, OH, OK, OR, SD, TN, TX, WA, and WI between 7/31/25 and 8/16/25. The affected KROGER Mercado brand shrimp 2lb. was sold at Baker's, Gerbes, Jay C, Kroger, Mariano s, Metro Market, Pay Less Supermarkets, and Pick n Save in AL, AR, GA, IL, IN, KS, KY, MI, MO, MS, NE, OH, SC, TN, VA, WI, WV between 7/24/25 and 8/11/25.
Firm state
WA
Product quantity
22,500 cases
Initiated by
Voluntary: Firm initiated
SPEQ quality domain
Environmental Monitoring
Reason for recall

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

Product description

AquaStar Cocktail Shrimp, 4oz. shrimp/2oz. cocktail sauce. Each case consists of 6x6 oz packages, UPC 19434612191. Distributed by Aqua Star, Seattle, WA. Farm Raised Product of Indonesia. Master cases distributed to distributors in frozen condition. AquaStar Cocktail Shrimp, 4oz. shrimp/2oz. cocktail sauce, net wt. 6oz. UPC 19434612191. Distributed by Aqua Star, Seattle, WA. Farm Raised Product of Indonesia. 6oz packages sold to consumers at Walmart as refrigerated product.

Code / lot info

***Information on master cases distributed frozen to distributors: Lot Code: 10662 5104 Best If Used By 4/14/2027 Lot Code: 10662 5105 Best If Used By 4/15/2027 Lot Code: 10662 5106 Best If Used By 4/16/2027 Lot Code: 10662 5107 Best If Used By 4/17/2027 Lot Code: 10662 5124 Best If Used By 5/4/2027 Lot Code: 10662 5125 Best If Used By 5/5/2027 ***Information on 6oz plastic trays sold at Walmart as refrigerated product: Lot Code: 10662 5106 Lot Code: 10662 5107 Lot Code: 10662 5124 Lot Code: 10662 5125 Use By Dates range from 8/9/25 to 8/26/25.

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Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.