CLASS I Food recall · Reported 22 Oct 2025 · FDA Enforcement Report

Haifa Cold Smoked Salmon recalled by D & M Smoked Fish

D & M Smoked Fish is recalling Haifa Cold Smoked Salmon, distributed in 7 states. The recall was initiated on 17 Sep 2025 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot # 219 UPC: 8 32007 00002 4
Quantity recalled2022 pieces

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
H-0032-2026
FDA event ID
97633
Recalling firm
D & M Smoked Fish, Jamaica, NY
Classification
Class I
Status
Terminated
Recall initiated
17 Sep 2025
FDA classified
10 Oct 2025
Reported
22 Oct 2025
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Listeria
Product category
Salmon

Timeline

17 Sep 2025Recall initiated by company
10 Oct 2025Classified by FDA+23 days
22 Oct 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Contaminated with Listeria monocytogenes

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

Haifa COLD SMOKED SALMON 8 OZ.

Where it was distributed

NY, NJ, PA, WA, CA, IL, FL

CaliforniaFloridaIllinoisNew JerseyNew YorkPennsylvaniaWashington

Questions about this recall

Why was it recalled?

Contaminated with Listeria monocytogenes

Which lots are affected?

Lot # 219 UPC: 8 32007 00002 4

Where was it sold?

NY, NJ, PA, WA, CA, IL, FL

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

1 other product · FDA event 97633
ReportedClassRecallCompanyReasonWhere
CLASS IHaifa Cold Smoked Seabass recalled by D & M Smoked FishHaifa ColdD & M Smoked FishListeria7 states

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