RecallRadar
High RiskReported October 22, 2025

Haifa COLD SMOKED SALMON 8 OZ.

Recalled by D & M Smoked Fish, Inc.

Food recall

D & M Smoked Fish, Inc.

Class I — most serious

There is a reasonable chance that using this product could cause serious health problems or death.

See all recalls involving Listeria

D & M Smoked Fish, Inc. has recalled Haifa COLD SMOKED SALMON 8 OZ., according to data published by the U.S. Food and Drug Administration (FDA). The recall was reported on October 22, 2025 and was initiated on September 17, 2025. It is classified as a Class I recall, which means there is a reasonable chance that using this product could cause serious health problems or death.

Below is a plain-English summary of what was recalled, why it was recalled, how to tell whether you have the affected product, and what steps you can take. For the complete and most current details, you can view the FDA record linked further down this page.

What was recalled?

This recall covers Haifa COLD SMOKED SALMON 8 OZ., with approximately 2022 pieces affected. The company behind the recall is D & M Smoked Fish, Inc., based in Jamaica, NY. The FDA describes the product as: “Haifa COLD SMOKED SALMON 8 OZ.”

Why was Haifa COLD SMOKED SALMON 8 OZ. recalled?

According to the FDA, the stated reason for the recall is: “Contaminated with Listeria monocytogenes.” In plain terms, this recall relates to Listeria.

Listeria monocytogenes is a bacterium that can grow even at refrigerator temperatures, which makes it a particular concern in ready-to-eat foods. Health authorities warn that it can cause a serious infection called listeriosis, and that pregnant people, newborns, older adults, and those with weakened immune systems are especially vulnerable. This is why products potentially contaminated with Listeria are often recalled quickly.

What should you do?

If you think you may have bought Haifa COLD SMOKED SALMON 8 OZ., compare it against the product description and identifying codes (Lot # 219 UPC: 8 32007 00002 4) before using it.

The general guidance for a matching product is to stop using it and follow the instructions in the official FDA recall notice, which may include a repair, replacement, refund, or safe disposal. When in doubt, contact D & M Smoked Fish, Inc. or your local health authority.

About this recall

This recall was distributed in NY. RecallRadar summarizes recall information from public FDA data to make it easier to understand. We are an independent service and are not affiliated with the FDA or any government agency, so please always refer to the official source for the authoritative record — and note the “last synced” date shown on this page, since recall details can change over time.

Full recall details

Status
Terminated
Date reported
October 22, 2025
Recall started
September 17, 2025
Distributed in
NY
What was recalled
Haifa COLD SMOKED SALMON 8 OZ.
Why it was recalled (as stated by the FDA)
Contaminated with Listeria monocytogenes
How to identify the affected product
Lot # 219 UPC: 8 32007 00002 4
Amount recalled
2022 pieces

What you can do

Check whether any product you have matches the description and codes above. If it does, stop using it and follow the instructions in the official recall notice. When in doubt, contact the company or your local health authority.

Quick answers

Why was Haifa COLD SMOKED SALMON 8 OZ. recalled?+

According to the FDA: Contaminated with Listeria monocytogenes

How serious is this recall?+

Class I — most serious. There is a reasonable chance that using this product could cause serious health problems or death.

What should I do if I have Haifa COLD SMOKED SALMON 8 OZ.?+

Compare your product against the description and identifying codes on this page. If it matches, stop using it and follow the instructions in the official recall notice — this usually means returning it for a refund or discarding it. When in doubt, contact the company or your local health authority.

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View the official FDA record

Opens the U.S. Food and Drug Administration (FDA) data for this recall.

Recall number: H-0032-2026. Information last synced from the FDA on July 5, 2026.

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