Irvington Seafood Claw Crab Meat packaged in 1lb plastic cups. 40 lb cases
Summary
The FDA issued a Class I for Irvington Seafood Claw Crab Meat packaged in 1lb plastic cups. 40 lb cases by Irvington Seafood, Inc. dba ISF, Inc.. Reason: Listeria monocytogenes identified in finished product testing..
Details
Source
Food Recall
External ID
F-1344-2024
Action Date
2024-06-19
Status
Terminated
Category
food
Product Description
Irvington Seafood Claw Crab Meat packaged in 1lb plastic cups. 40 lb cases
Lot/Code Info: Batch 133 Packer No AL 111-C Expiration 05/26/24
Quantity Affected: 83 lbs
Reason for Recall
Listeria monocytogenes identified in finished product testing.
Distribution
MS and AL
Type: Voluntary: Firm initiated
Recall Initiated: 2024-05-17
Company
Irvington, AL
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 88 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-1344-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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