Frozen Cooked Medium Shrimp Peeled & Deveined, Tail Off-White Shrimp; 1 lbs retail plastic bag. UPC: 041220333035
Summary
The FDA issued a Class II for Frozen Cooked Medium Shrimp Peeled & Deveined, Tail Off-White Shrimp; 1 lbs reta by H & N Group Inc.. Reason: Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137).
Details
Source
Food Recall
External ID
H-0516-2026
Action Date
2026-02-25
Status
Terminated
Category
food
Product Description
Frozen Cooked Medium Shrimp Peeled & Deveined, Tail Off-White Shrimp; 1 lbs retail plastic bag. UPC: 041220333035
Lot/Code Info: " Lot EA14 25118, bearing a Best By date of October 28, 2026 " Lot EA14 25119, bearing a Best By date of October 29, 2026
Quantity Affected: 378 cases (3,780 units)
Reason for Recall
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Distribution
Product was distributed to a single retail consignee with multiple locations (~30) in the greater Houston and Gulf Coast areas.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-02-09
Company
Vernon, CA
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 33 food recalls issued in the same week, part of 204 food-related FDA actions this month.
H & N Group Inc. has 2 FDA actions in our database, including 2 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 (H & N Group Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does H & N Group Inc. have FDA actions?
H & N Group Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0516-2026" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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