Frozen shrimp in bulk packaging. 20 lbs (10 x 2 lbs blocks); 20 lbs (20 x 1 lbs blocks); 9 lbs case UPC# SH0176; SH0430
Summary
The FDA issued a Class II for Frozen shrimp in bulk packaging. 20 lbs (10 x 2 lbs blocks); 20 lbs (20 x 1 lbs 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-0548-2025
Action Date
2025-09-03
Status
Terminated
Category
food
Product Description
Frozen shrimp in bulk packaging. 20 lbs (10 x 2 lbs blocks); 20 lbs (20 x 1 lbs blocks); 9 lbs case UPC# SH0176; SH0430; SH0320; SH0369; SH0370
Lot/Code Info: Lot numbers: Line Entries 594-0398297-4; 594-0398336-0; 594-0398335-2; 594-0398337-8 E14 25106 HN521 139; E14 25107 HN521 139; E14 25108 HN522 080; E14 25109 HN522 080; E14 25118 HN523 139; E14 25119 HN523 139; E14 25120 HN524 080; E14 25122 HN524 080; Line Entries 594-0398298-2; 594-0397189-4; E14 25103 HN520 080; E14 25105 HN520 080; E14 25125 HN526 080; E14 25126 HN526 080; Line Entries 594-0398543-1 13825 V20761 0064267 HN505 139; 13925 V20761 0064267 HN505 080 Line Entries 594-0397186-0 E14 25112 HN514 139; E14 25113 HN514 139 Line Entries 594-0397230-6-10002/1 HN50313925132
Quantity Affected: 17,214 cases across all brands
Reason for Recall
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Distribution
Product is distributed to various retail grocery stores primarily on the East Coast.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-08-12
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 43 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-0548-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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