RecallHawk
Class I Recall

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

Irvington Seafood, Inc. dba ISF, Inc.

Summary

The FDA issued a Class I for Irvington Seafood Crabmeat: Jumbo, Lump, Finger, Claw packaged in 16oz plastic c by Irvington Seafood, Inc. dba ISF, Inc.. Reason: possible contamination of Listeria monocytogenes.

Details

Source

Food Recall

External ID

F-1349-2022

Action Date

2022-06-29

Status

Terminated

Category

food

Product Description

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

Lot/Code Info: 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

Quantity Affected: 12,838 lbs total

Reason for Recall

possible contamination of Listeria monocytogenes

Distribution

AL, GA, LA, MS

Type: Voluntary: Firm initiated

Recall Initiated: 2022-06-01

Context & Analysis

This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.

This was one of 78 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Irvington Seafood, Inc. dba ISF, Inc. has 5 FDA actions in our database, including 5 recalls.

Frequently Asked Questions

What is a Class I recall?

A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.

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 (Irvington Seafood, Inc. dba ISF, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Irvington Seafood, Inc. dba ISF, Inc. have FDA actions?

Irvington Seafood, Inc. dba ISF, Inc. has 5 FDA actions in our database, including 5 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1349-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

Want to know the moment something like this happens?

Get alerts for food

Related Actions