Recall record at a glance
| Official record | H-0583-2025 |
|---|---|
| Category | Food Recalls |
| Classification | Class II |
| FDA record status | Ongoing |
| Recalling firm | Admiralty Island Fisheries Inc dba AquaStar (USA) Corp. |
| Report date | Sep 24, 2025 |
| Recall initiation date | Aug 14, 2025 |
| Quantity | 22,500 cases |
| Location | Seattle, WA, United States |
Official 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.
Why the product was recalled
Product may be contaminated with Cesium-137 (Cs-137).
Distribution information
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.
How to read the classification
FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.