Food Recall Check
Class I · High risk Terminated Initiated Jun 1, 2022 (4 years ago)

Irvington Seafood Crabmeat recall

Recalled by Irvington Seafood, Inc. dba ISF, Inc. · Irvington, AL, United States

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

possible contamination of Listeria monocytogenes

Pathogen: Listeria

Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.

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

Irvington Seafood Crabmeat: Jumbo, Lump, Finger, Claw packaged in 16oz plastic cups - 40lbs per case

Quantity: 12,838 lbs total

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.

Batch Number: 130, 131, 132, 134, 137, 139, 141, 144, 145, 146, 148, 150 Processing Dates: 05/09/22, 05/10/22, 05/11/22, 05/12/22, 05/14/22, 05/17/22, 05/19/22, 05/21/22, 05/24/22, 05/25/22, 05/26/22, 05/28, 05/30/22 Manufacturer Code: AL 111-C/22

Where it was sold

Alabama Georgia Louisiana Mississippi

FDA's distribution note: AL, GA, LA, MS

Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. 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
Irvington Seafood, Inc. dba ISF, Inc.
Initiated by
Voluntary: Firm initiated
Recall initiated
Jun 1, 2022
In FDA report of
Jun 29, 2022
Terminated
May 19, 2023
FDA recall number
F-1349-2022 · event 90342
Official record
FDA enforcement report search

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