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Admiralty Island Fisheries Inc dba AquaStar (USA) Corp.
FDA recall H-0583-2025 · Class II · reported 2025-09-24 · Ongoing
- Product
- 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.
- Reason
- Product may be contaminated with Cesium-137 (Cs-137).
- Quantity
- 22,500 cases
- 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 location
- WA, United States
- Initiated
- Voluntary: Firm initiated
- First notice
- Recall started
- 2025-08-14
- Code 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.
Source: U.S. Food and Drug Administration, openFDA Food Enforcement database (openFDA Food Enforcement, imported 2026-09). The FDA does not validate openFDA data for completeness or accuracy. This is a record of an enforcement action, not safety advice.