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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Critical RiskFDA Food
Food & Beverages/Packaged & Processed

Bakkafrost and Hiddenfjord Salmon and Tuna Recalled for Listeria

Agency Publication Date: January 26, 2024
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Summary

Ocean Group Inc. is recalling 18,208 units of various fresh salmon and tuna products because they may be contaminated with Listeria monocytogenes. The recall includes 18,042 salmon fillet pieces and 166 pieces of tuna sold under brands like Bakkafrost and Hiddenfjord, with expiration dates between December 11 and December 29. The potential contamination was discovered through environmental testing conducted by the FDA. No illnesses or injuries have been reported to date. These products were distributed in California.

Risk

The products may be contaminated with Listeria monocytogenes, a bacterium that can cause serious and sometimes fatal infections. High-risk individuals include young children, the elderly, and those with weakened immune systems. In pregnant women, Listeria infection can cause miscarriages and stillbirths.

What You Should Do

  1. This recall affects various salmon and tuna products sold under the Bakkafrost (Faroe Islands, Scottish), Hiddenfjord, Hawaii Tuna, Canada, Norway, Spain, Japan, and Mexico brands with expiration dates ranging from December 11 to December 29.
  2. Identify affected products by checking for specific item numbers on the packaging, including codes like 202225, 202002, 201000, and TUNA001B. See the Affected Products section below for the full list of affected codes.
  3. Return the product to the place of purchase for a refund, throw it away, or contact Ocean Group Inc. directly for further instructions.
  4. Call the FDA Consumer Complaint hotline at 1-888-723-3332 (1-888-SAFEFDA) if you have additional questions regarding this recall.

Your Remedy Options

You have 2 options:

๐Ÿ’ฐOption 1: Full Refund
How to: Return the product to the place of purchase for a full refund, or contact the manufacturer or supplier for further instructions
๐Ÿ—‘๏ธOption 2: Dispose of Product
How to: Throw the product away.

Affected Products

Product: Salmon Fillet Products (Bakkafrost, Hiddenfjord, Canada, Norway)
Variants: Bakkafrost Faroe Islands, Bakkafrost Scottish, Hiddenfjord Faroe Islands, Canada Fillet, Norway Fillet, 6/7KG, 5/6KG, 7/8KG, 8/9KG, 10/12, 12/14, 14/16, 16/18, 18/20, Trim C, Trim E, Trim B
Item Code:
202225
202002
202012
202022
202032
SAL005
202020
202213
202100
202110
202120
202130
202140
202240
20270
202004
202271
202014
202019
202272
202024
202034
202011
202021
Date Ranges: Expiration date: Dec 11-Dec 29

Quantity: 18,042 fillet pieces. Recall #: F-0804-2024.

Product: Tuna Portions and Scraps (Hawaii, Spain, Japan, Mexico)
Variants: Hawaii #1 USA, Wild Yellowfin, Bigeye #2 Grade, Bluefin Spain, Bluefin Japan, Tesshin Scraps, Bluefina Mexico, Boston Bluefin
Item Code:
201000
201002
201200
201300
201301
201304
201508
201900
TUNA001B
TUNA001C
TUNA001D
TUNA001E
TUNA001NZ
TUNA001W
Date Ranges: Expiration date: Dec 11-Dec 29

Quantity: 166 pieces. Recall #: F-0805-2024.

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93716
Status: Resolved
Manufacturer: Ocean Group Inc.
Sold By: Ocean Group Inc.
Manufactured In: United States, Faroe Islands, United Kingdom, Canada, Norway, Spain, Japan, Mexico
Units Affected: 2 products (18,042 fillet pieces; 166 pieces)
Distributed To: California

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.