FDA recall record

Southwind Foods LLC dba Great American Seafood Arctic Shores recall — FDA H-0112-2026

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original…

Class IIclassification
H-0112-2026official record ID
Oct 29, 2025report date

Recall record at a glance

Official recordH-0112-2026
CategoryFood Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmSouthwind Foods LLC dba Great American Seafood Imports Co.
Report dateOct 29, 2025
Recall initiation dateSep 23, 2025
Quantity93,122 cases (1,275,765 lbs) Total
LocationCarson, CA, United States

Official product description

Arctic Shores; Best Yet; Great American; Master Catch branded Frozen cooked shrimp; 2lbs; 1lbs; 12oz bags; UPC: 041130810497; 041130810411; 041130811685; 041130810817; 042187002705; 829944012623; 042187002712; 829944012630; 042187002729; 829944011510; 041130812385; 042187002736; 042187002736; 829944013576; 829944012616; 829944093073; 041130810466; 041130810473; 042187002743; 829944011541; 717544137047; 829944012173; 829944002631; 042187002750; 829944011565; 829944010674; 829944011381; 042187002774; 829944092540; 041130812392

Why the product was recalled

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original recall.

Distribution information

Distribution includes 26 domestic retail consignees across the following states: Alabama, Arizona, California, Colorado, Connecticut, Florida, Georgia, Hawaii, Idaho, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Michigan, Minnesota, Missouri, Montana, Nebraska, Nevada, New Jersey, New Mexico, New York, Ohio, Oregon, Pennsylvania, Rhode Island, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, and Wyoming.

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: Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit.

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.

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