16/25 Frozen Cooked Tail-On Farm Raised Shrimp; 12oz clear plastic retail bag. UPC: 011110649812 51/60 Frozen Cooked Ta
Summary
The FDA issued a Class II for 16/25 Frozen Cooked Tail-On Farm Raised Shrimp; 12oz clear plastic retail bag. U by Lawrence Wholesale LLC. Reason: Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137).
Details
Source
Food Recall
External ID
H-0639-2025
Action Date
2025-10-08
Status
Terminated
Category
food
Product Description
16/25 Frozen Cooked Tail-On Farm Raised Shrimp; 12oz clear plastic retail bag. UPC: 011110649812 51/60 Frozen Cooked Tail-On Farm Raised Shrimp; 32oz clear plastic retail bag. UPC: 011110967015
Lot/Code Info: 12oz Lot numbers: 11925-H3A1, 12025-H3A1 Best By: 04/28/2027, 04/29/2027 32oz Lot numbers: 12225-H3A1, 12325-H3A1 Best By: 05/01/2027, 05/02/2027
Quantity Affected: 4,871 cases
Reason for Recall
Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)
Distribution
Product was distributed to Kroger stores in the following states; Arizona, California, Colorado, Georgia, Kansas, Kentucky, Michigan, Nevada, Ohio, Oregon, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-09-16
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 39 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Lawrence Wholesale LLC 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 (Lawrence Wholesale LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Lawrence Wholesale LLC have FDA actions?
Lawrence Wholesale LLC 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-0639-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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