Food Recall Check
Class II · Moderate risk Terminated Initiated Sep 30, 2025 (12 months ago)

Oceans Kitchen IMITATION CRABMEAT SHREDDED Made From Wild Fish recall

Recalled by Ocean's Kitchen Corp. · Kent, WA, United States

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

Why it was recalled

The potential contamination with Clostridium botulinum, due to risk of temperature abuse during chilled storage at the firm.

Pathogen: Botulism

Clostridium botulinum toxin, a risk in improperly canned or under-processed foods.

The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.

What was recalled

Oceans Kitchen IMITATION CRABMEAT SHREDDED Made From Wild Fish, Refrigerated, vacuum package. Net wt. per bag 2.5 lbs. UPC 1 90456 75654 2. These 2.5lb. bags are not for retail sales. Each master case contains 12/2.5lbs. bags. Net wt. per case: 30lbs. UPC 14972195756549. Oceans Kitchen Corporation, 7622 S 188TH ST., KENT, WA 98032

Quantity: 496 cases (12/2.5lb. bags per 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.

USE BY OCT 23 2025 Best If Used By: 10/23/2025 Lot #CH062525 USE BY OCT 31 2025 Best If Used By: 10/31/2025 Lot # CH070325 USE BY NOV 6 2025 Best If Used By: 11/6/2025 Lot # CH070925

Where it was sold

Washington

FDA's distribution note: Distributed in WA

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
Ocean's Kitchen Corp.
Initiated by
Voluntary: Firm initiated
Recall initiated
Sep 30, 2025
In FDA report of
Oct 29, 2025
Terminated
Nov 19, 2025
FDA recall number
H-0140-2026 · event 97734
Official record
FDA enforcement report search

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