Ocean Group Inc. Recall: Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings.

🇺🇸 United States

1. December 29, 2023 - Recall initiated
2. February 7, 2024 - Reported by source
3. June 14, 2024 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0804-2024

Event ID

93716

Status

Terminated

Classification

Class I

Company

Ocean Group Inc.

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

Quantity

18,042 fillet pieces

Reason

Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings.

Recall initiation date

December 29, 2023

Report date

February 7, 2024

Classification date

Not published in this source record

Termination date

June 14, 2024

Distribution pattern

U.S. distribution: CA No foreign distribution.

UPC, lot, and code information

Expiration date: Dec 11-Dec 29

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Letter

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 93716 with 1 other product entry in Public Health Trace.

Responsible company: Ocean Group Inc.

Other recalls from Ocean Group Inc.

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
California	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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