201000 TUNA, HAWAII #1 USA W LB 201002 TUNA HAWAII #1 USA W LB 201200 TUNA FRESH, WILD Y/F,B/E #2 GRADE 201300 TUNA B
Summary
The FDA issued a Class I for 201000 TUNA, HAWAII #1 USA W LB 201002 TUNA HAWAII #1 USA W LB 201200 TUNA FRE by Ocean Group Inc.. Reason: Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings..
Details
Source
Food Recall
External ID
F-0805-2024
Action Date
2024-02-07
Status
Terminated
Category
food
Product Description
201000 TUNA, HAWAII #1 USA W LB 201002 TUNA HAWAII #1 USA W LB 201200 TUNA FRESH, WILD Y/F,B/E #2 GRADE 201300 TUNA BLUEFIN SPAIN SPA F LB 201301 TUNA BLUEFIN SPAIN (SE) SPAIN F LB 201304 TUNA BLUEFIN SPAIN G&G SPAIN F LB 201508 TUNA BLUE FIN GG JAPAN FR JPN F LB 201900 TUNA, FRESH SCRAPS "TESSHIN" WILD LB TUNA001B TUNA, FRESH "BLUEFINA" MEXICO FARM LB TUNA001C TUNA, FRESH TUNA BLUEFIN PORTION (MEXICO) FARM/LB TUNA001D TUNA BLUE FIN MEXICO SMALL FR MEX FLB TUNA001E TUNA BLUE FIN *BACKSIDE* MEXICO FARM LB TUNA001NZ TUNA, BLUE FIN LOCAL WILD LB TUNA001W TUNA, FRESH BOSTON BLUEFIN WILD LB
Lot/Code Info: Expiration date: Dec 11-Dec 29
Quantity Affected: 166 pieces
Reason for Recall
Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings.
Distribution
U.S. distribution: CA No foreign distribution.
Type: Voluntary: Firm initiated
Recall Initiated: 2023-12-29
Company
Los Angeles, CA
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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Ocean Group Inc. has 3 FDA actions in our database, including 3 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 (Ocean Group Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Ocean Group Inc. have FDA actions?
Ocean Group Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0805-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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