Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 16, 2025 (13 months ago)

Shrimp Cocktail Bowl recall

Recalled by Lawrence Wholesale LLC · Vernon, CA, United States

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Product manufactured under insanitary conditions whereby it may have been contaminated with Cesium-137 (Cs-137)

These are failures of the safety steps that keep food safe - cooking, pasteurising, keeping cold, sealing - even when no contaminant has yet been found. All processing & sanitation problems recalls.

What was recalled

Shrimp Cocktail Bowl; 7oz clear plastic retail packaging. UPC: 011110622952 Shrimp Cocktail Bowl; 17oz clear plastic retail packaging. UPC: 011110624840

Quantity: 8,400 cases (12 units/case)

Food: Seafood & fish

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

7oz Lot numbers: 11325-H3A1, 11425-H3A1, 11525-H3A1, 11625-H3A1 Best By: 04/22/2027, 04/23/2027, 04/24/2027, 04/25/2027 17oz Lot numbers: 13725-H3A1, 13825-H3A1 Best By: 05/16/2027, 05/17/2027

Where it was sold

Arizona California Colorado Georgia Kansas Kentucky Michigan Nevada Ohio Oregon Tennessee Texas Utah Virginia Washington Wisconsin

FDA's distribution note: 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.

Check the codes, then return or discard. Class II means eating it may cause temporary or reversible health problems. If your package matches the recalled codes, do not eat it - return it to the store or throw it away. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Lawrence Wholesale LLC
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 16, 2025
In FDA report of
Oct 8, 2025
Terminated
Feb 5, 2026
FDA recall number
H-0638-2025 · event 97632
Official record
FDA enforcement report search

Also recalled with it (1 more product)

FDA files each product of one recall action separately; these share the same FDA event.

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