202225 SALMON BAKKA FROST FILLET 6/7KG FR FRO F LB 202002 SALMON BAKKAFROST FAROE ISLANDS 5/6KG FR FRO F LB 202012 SAL
Summary
The FDA issued a Class I for 202225 SALMON BAKKA FROST FILLET 6/7KG FR FRO F LB 202002 SALMON BAKKAFROST FAR 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-0804-2024
Action Date
2024-02-07
Status
Terminated
Category
food
Product Description
202225 SALMON BAKKA FROST FILLET 6/7KG FR FRO F LB 202002 SALMON BAKKAFROST FAROE ISLANDS 5/6KG FR FRO F LB 202012 SALMON BAKKAFROST FAROE ISLANDS 6/7KG FR FRO F LB 202022 SALMON BAKKAFROST FAROE ISLANDS 7/8KG FR FRO F LB 202032 SALMON BAKKAFROST FAROE ISLANDS 8/9KG FR FRO F LB SAL005 SALMON BAKKAFROST SCOTTISH FLT TRIM "C" 6/7KG FR GBR F LB 202020 SALMON BAKKAFROST SCOTTISH 7/8KG FR GBR F LB 202213 SALMON CANADA FLT TRIM "E" 10/12 FR CAN F LB 202100 SALMON CANADA 10/12 FR CAN F LB 202110 SALMON CANADA 12/14 FR CAN F LB 202120 SALMON CANADA 14/16 FR CAN F LB 202130 SALMON CANADA 16/18 FR CAN F LB 202140 SALMON CANADA 18/20,20+ FR CAN F LB 202240 SALMON CANADA FILLET 12/14 FR CAN F LB 20270 SALMON HIDDENFJORD FAROE ISLANDS 5/6KG FILLET "E" FR F LB 202004 SALMON HIDDENFJORD FAROE ISLANDS 5/6KG FR F LB 202271 SALMON HIDDENFJORD FAROE ISLANDS 6/7KG FILLET "E" FR F LB 202014 SALMON HIDDENFJORD FAROE ISLANDS 6/7KG FR F LB 202019 SALMON HIDDENFJORD FAROE ISLANDS 6/7KG FILLET "B" FR F LB 202272 SALMON HIDDENFJORD FAROE ISLANDS 7/8KG FILLET "E" FR F LB 202024 SALMON HIDDENFJORD FAROE ISLANDS 7/8KG FR F LB 202034 SALMON HIDDENFJORD FAROE ISLANDS 8/9KG FR F LB 202011 SALMON NORWAY 6/7KG FR NOR F LB 202021 SALMON NORWAY 7/8KG FR NOR F LB
Lot/Code Info: Expiration date: Dec 11-Dec 29
Quantity Affected: 18,042 fillet 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-0804-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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