Central Seafoods 30# case of IQF whole octopus. Three item codes / GTIN numbers depending on size of individual octopu
Summary
The FDA issued a Class I for Central Seafoods 30# case of IQF whole octopus. Three item codes / GTIN number by CenSea Inc. Reason: Product tested positive for Salmonella.
Details
Source
Food Recall
External ID
F-1606-2023
Action Date
2023-10-04
Status
Terminated
Category
food
Product Description
Central Seafoods 30# case of IQF whole octopus. Three item codes / GTIN numbers depending on size of individual octopus: Item 10400: 2-4 pound whole octopus, GTIN 1 00 70041 20007 0. Item 10432: 4-6 pound whole octopus, GTIN 1 00 70041 20008 7. Item 10460: 6-8 pound whole octopus, GTIN 1 00 70041 20009 4.
Lot/Code Info: Lot# 22306314
Quantity Affected: 281 cases
Reason for Recall
Product tested positive for Salmonella
Distribution
OH, FL, GA, IL
Type: Voluntary: Firm initiated
Recall Initiated: 2023-09-01
Company
Northbrook, IL
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 185 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (CenSea Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does CenSea Inc have FDA actions?
This is the only FDA action we have on record for CenSea Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1606-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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