D & M Smoked Fish, Inc. food recall: Haifa COLD SMOKED SALMON 8 OZ
Key facts
- Agency
- U.S. Food and Drug Administration (FDA)
- Program
- Food
- Classification
- Class I
- Status
- Terminated
- Event ID
- 97633
- Recall initiated
- Sep 17, 2025
- Classified by FDA
- Oct 10, 2025
- Posted in Enforcement Report
- Oct 22, 2025
- Terminated
- Apr 17, 2026
- Recalling firm
- D & M Smoked Fish, Inc.
- Firm location
- Jamaica, NY, United States
- Initiated by
- Voluntary: Firm initiated
- Firm notified customers by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Products in this event
- 2
What to do
Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.
Reason for recall
Contaminated with Listeria monocytogenes
What the classification means
- Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.
About this recall
The firm started this recall on Sep 17, 2025. FDA classified it 23 days later, on Oct 10, 2025. This recall event covers 2 separate products, each with its own FDA recall number. Distribution reported by FDA: NY, NJ, PA, WA, CA, IL, FL D & M Smoked Fish, Inc. has 2 recalls in our records.
Recalled products (2)
H-0032-2026 Class I Terminated
Haifa COLD SMOKED SALMON 8 OZ.
Codes / lots: Lot # 219 UPC: 8 32007 00002 4
Quantity: 2022 pieces
H-0033-2026 Class I Terminated
Haifa COLD SMOKED SEABASS 8 OZ
Codes / lots: Lot # 212 UPC: 8 32007 00151 9
Quantity: 348 pieces
Source and freshness
- Source
- U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
- Official notice
- FDA Enforcement Report, event 97633
- Raw record
- openFDA API (JSON)
- Dataset last updated by FDA
- Nov 3, 2026
- Imported by RecallRadar
- Nov 4, 2026
Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.