Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788
Summary
The FDA issued a Class II for Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788 by Southwind Foods LLC dba Great American Seafood Imports Co.. Reason: Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137). This is an expansion to the original .
Details
Source
Food Recall
External ID
H-0115-2026
Action Date
2025-10-29
Status
Terminated
Category
food
Product Description
Tovala branded Frozen raw phosphate free shrimp; 5oz IQF bag UPC: 829944085788
Lot/Code Info: Best By Date: 4/27/2027
Quantity Affected: 93,122 cases (1,275,765 lbs) Total
Reason for Recall
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
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.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-23
Company
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 91 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Southwind Foods LLC dba Great American Seafood Imports Co. has 7 FDA actions in our database, including 7 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Southwind Foods LLC dba Great American Seafood Imports Co.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Southwind Foods LLC dba Great American Seafood Imports Co. have FDA actions?
Southwind Foods LLC dba Great American Seafood Imports Co. has 7 FDA actions in our database, including 7 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0115-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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