Ocean Group Inc. recalls specific tuna products due to potential Listeria contamination found in FDA environmental sampling. Consumers should check product labels for affected items and contact the company for details.
Potential L. mono contamination as a result of FDA environmental sampling revealing positive findings.
Ocean Group Inc. is recalling several tuna products that may contain Listeria bacteria. This contamination risk could lead to serious health issues if consumed.
FDA environmental sampling detected Listeria bacteria in some tuna products. Listeria can cause serious infections, especially in pregnant women, newborns, and people with compromised immune systems.
Consumers who purchased the recalled tuna products from the listed brands and model numbers are affected. Those with weakened immune systems are at higher risk.
Check product labels for the specific model numbers listed in the recall: 201000, 201002, 201200, 201300, 201301, 201304, 201508, 201900, TUNA001B, TUNA001C, TUNA001D, TUNA001E, TUNA001NZ, TUNA001W. These products were sold in the US and Mexico with specific expiration dates.
Look for the specific model numbers listed in the recall notice on the tuna packaging.
Check the product label for the model numbers listed: 201000, 201002, 201200, 201300, 201301, 201304, 201508, 201900, TUNA001B, TUNA001C, TUNA001D, TUNA001E, TUNA001NZ, TUNA001W.
The recall does not specify a remedy, so contact Ocean Group Inc. directly for further instructions.
Listeria can cause serious infections, especially in pregnant women, newborns, and people with weakened immune systems.
We’ve drafted a message you can send Ocean Group to request your refund or repair — edit it as you like.
Subject: Recall F-0805-2024 — Ocean Group Ocean Group Hello, I own a Ocean Group that is covered by recall F-0805-2024 from Ocean Group. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
