Recall record at a glance
| Official record | F-0804-2024 |
|---|---|
| Category | Food Recalls |
| Classification | Class I |
| FDA record status | Terminated |
| Recalling firm | Ocean Group Inc. |
| Report date | Feb 7, 2024 |
| Recall initiation date | Dec 29, 2023 |
| Quantity | 18,042 fillet pieces |
| Location | Los Angeles, CA, United States |
Official 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
Why the product was recalled
Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings.
Distribution information
U.S. distribution: CA No foreign distribution.
How to read the classification
FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.
Additional record details
Recall type: Voluntary: Firm initiated. Initial notification: Letter.
What to do next
If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.
About this record
Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.
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