Class IITerminatedVoluntary: Firm initiated
Southwind Foods LLC dba Great American Seafood Imports Co.: food recall H-0603-2025
Southwind Foods LLC dba Great American Seafood Imports Co. of Carson, CA recalled Sand Bar; Great American; and First Street branded Frozen raw shrimp; 2 pound plastic bag; UPC#: 011110641182;… Reason: Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). The FDA listed it as Class II in its Enforcement Report dated Sep 24, 2025; distribution: Alabama, Arizona, California, Massachusetts, Minnesota, Pennsylvania, Utah, Virginia, Washington.
Record status as published: Terminated (terminated May 28, 2026). openFDA data last updated Oct 21, 2026.
Have this product? Check FDA.gov and your retailer. This page reproduces an FDA Enforcement Report record and is not a public alert. Look for the firm's recall notice on the FDA's recalls page, or ask the store where you bought it what to do. If you think you got sick from a food, contact a health care provider.
Recall details
- Product
- Sand Bar; Great American; and First Street branded Frozen raw shrimp; 2 pound plastic bag; UPC#: 011110641182; 829944010612; 041512179471; 829944010698; 8299440106636
- Product quantity
- 11,081 cases across all products and brands
- Reason for recall
- Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
- Codes, lots and dates on the package
- Lot# 087305; 125143; 130632; 128267
- Distribution pattern
- Product was distriburted to the following states: Alabama, Arizona, California, Massachusetts, Minnesota, Pennsylvania, Utah, Virginia, and Washington state. No foreign distribution.
- Recalling firm
- Southwind Foods LLC dba Great American Seafood Imports Co., Carson, CA
- Classification
- Class II — the FDA uses this class for a situation in which using or being exposed to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
- Voluntary or mandated
- Voluntary: Firm initiated
- How the firm first notified customers
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Dates
| Event | Date |
|---|---|
| Recall initiated by the firm | Aug 19, 2025 |
| Classified by the FDA | Sep 12, 2025 |
| Published in the Enforcement Report | Sep 24, 2025 |
| Terminated | May 28, 2026 |
Other products in the same recall event
The FDA groups related products under one recall event (event 97476).
- H-0604-2025 — Best Yet; Arctic Shores; and Great American branded Frozen cooked shrimp; 1 Pound/ 12 OZ/ 6 OZ/ 2 Pound plastic bag; (Various Brands) UPC#: 042187002736; 042187002743; 041130812392; 041130810497; 041130810411;…
Other recalls by Southwind Foods LLC dba Great American Seafood Imports Co.
- H-0116-2026 · Oct 29, 2025 · Class II — Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- H-0115-2026 · Oct 29, 2025 · Class II — Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- H-0114-2026 · Oct 29, 2025 · Class II — Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- H-0113-2026 · Oct 29, 2025 · Class II — Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
- H-0112-2026 · Oct 29, 2025 · Class II — Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.
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Sources
- U.S. Food and Drug Administration, openFDA food enforcement reports, recall number H-0603-2025 (openFDA record). Data provided by the U.S. Food and Drug Administration (https://open.fda.gov).
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service. The FDA does not endorse OpenPlate.