D & M Smoked Fish, Inc. recalls "Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z."
D & M Smoked Fish recalls specific turbot smoked fish products contaminated with Listeria monocytogenes. Consumers should check lot codes and UPC numbers for affected items.
Stop using this now
May be contaminated with Listeria monocytogenes
Contact the company & request your remedy
What happened, in plain English
D & M Smoked Fish is recalling certain turbot smoked fish products due to potential Listeria monocytogenes contamination. This bacteria can cause serious illness, so affected consumers should stop using the product. Read more at govinfonow.com/recall/13544-d-m-smoked-fish-recall-listeria-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/13544-d-m-smoked-fish-recall-listeria-contamination-risk · Updated October 4, 2026 · FDA enforcement record: FDA #F-0505-2022
Cite this page
“D & M Smoked Fish Recall: Listeria Contamination Risk.” GovInfoNow, updated October 4, 2026. https://govinfonow.com/recall/13544-d-m-smoked-fish-recall-listeria-contamination-risk. Based on FDA recall #F-0505-2022 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-0505-2022%22&limit=1).
Why it’s dangerous
Listeria monocytogenes is a bacteria that can cause severe infections, especially in pregnant women, newborns, and people with weakened immune systems. Contaminated food can lead to serious illness if eaten.
Who’s affected
Consumers who purchased the recalled turbot smoked fish products with lot codes 246, 97, 223, 299, or 321 or UPC 832007001106 are affected. Pregnant women, newborns, and immunocompromised individuals are at higher risk.
How to tell if you have this one
Check the product label for lot codes 246, 97, 223, 299, or 321 or UPC code 832007001106. The product is labeled as 'Haifa Smoked Fish and Caviar' or 'Turbot Cold Smoked' with a net weight of 8 oz.
- Brand
D & M Smoked Fish- Product
"Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z."- Category
Food
What to do — step by step
Check Product Label
Look for lot codes 246, 97, 223, 299, or 321 or UPC code 832007001106 on the product label.
Questions people ask
Is this product safe to eat?
No, the product may be contaminated with Listeria monocytogenes, which can cause serious illness. Do not eat the recalled product.
What should I do if I have the recalled product?
Check the product label for the lot codes or UPC code. If it matches, stop using it immediately and contact the manufacturer for further instructions.
Who is most at risk from this contamination?
Pregnant women, newborns, and people with weakened immune systems are at higher risk of serious illness from Listeria monocytogenes.
Contact D & M Smoked Fish
We’ve drafted a message you can send D & M Smoked Fish to request your refund or repair — edit it as you like.
Subject: Recall F-0505-2022 — D & M Smoked Fish "Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z." Hello, I own a "Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z." that is covered by recall F-0505-2022 from D & M Smoked Fish. 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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Where this comes from
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.
- Official source: FDA Recall #F-0505-2022 (December 21, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-0505-2022 to see it in context.
- Plain-language summary written by qwen3:4b on October 4, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.