Recalls / Class II
Class IIH-0112-2026
Product
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
- Type
- Food
- Affected lot / code info
- Best By Date: 4/18/2027; 4/19/2027; 4/20/2027; 4/21/2027; 4/22/2027; 4/23/2027; 4/28/2027; 4/29/2027; 5/05/2027; 5/10/2027; 5/14/2027; 5/16/2027; 5/17/2027; 5/18/2027; 5/19/2027; 5/20/2027; 5/21/2027; 5/22/2027; 5/23/2027; 5/24/2027; 5/25/2027; 5/26/2027; 5/27/2027; 6/12/2027; 6/17/2027;
- Quantity
- 93,122 cases (1,275,765 lbs) Total
Why it 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.
Recalling firm
- Firm
- Southwind Foods LLC dba Great American Seafood Imports Co.
- Notification channel
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Type
- Voluntary: Firm initiated
- Address
- 20644 S Fordyce Ave, Carson, California 90810-1018
Distribution
- Distribution pattern
- 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.
Timeline
- Recall initiated
- 2025-09-23
- FDA classified
- 2025-10-21
- Posted by FDA
- 2025-10-29
- Status
- Ongoing
Source: openFDA Food Enforcement endpoint. Recall record H-0112-2026. The FDA issues recall classifications as health-hazard assessments, not legal findings.