Food Recall Check
Class II · Moderate risk Terminated Initiated Oct 24, 2017 (9 years ago)

Chicken of the Sea Pasteurized Crabmeat Lump Blend recall

Recalled by Performance Food Group, Inc. · Mckinney, TX, United States

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

Why it was recalled

The firm is initiating a recall due to potential temperature abuse to product during transit.

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

Chicken of the Sea Pasteurized Crabmeat Lump Blend, Item #411820; Chicken of the Sea Pasteurized Crabmeat Claw, Item #370810; Jack's Catch Pasteurized Crabmeat Jumbo Lump Item #193980; Jack's Catch Pasteurized Crabmeat Lump, Item #199830. All packaged in 1 LB or 16 OZ tin cans.

Quantity: 353 cases (12 units 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.

Item #193980 Manufacturer Code Number: 93981-10 and Best by Date: 10/08/2018; Item #411820 Manufacturer Code Number: 411821238 and Best by Date(s): 09/02/2018; 10/28/2018; 11/08/2018; Item #370810 Manufacturer Code Number: 10843237008152 and Best by Date(s): 09/19/2018; 11/18/2018; Item #199830 Manufacturer Code Number: 93982-10 and Best by Date: 10/03/2018

Where it was sold

Colorado Louisiana Missouri Nebraska Oklahoma Texas

FDA's distribution note: TX, CO, LA, MO, OK, NE

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
Performance Food Group, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Oct 24, 2017
In FDA report of
Nov 22, 2017
Terminated
Dec 7, 2017
FDA recall number
F-0372-2018 · event 78365
Official record
FDA enforcement report search

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