"Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z."
Summary
The FDA issued a Class I for "Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z." by D & M Smoked Fish, Inc.. Reason: May be contaminated with Listeria monocytogenes.
Details
Source
Food Recall
External ID
F-0505-2022
Action Date
2022-01-26
Status
Terminated
Category
food
Product Description
"Haifa Smoked Fish and Caviar*** Turbot Cold Smoked***Net Wt 8 0z."
Lot/Code Info: lot code: 246, 97, 223, 299, 321 UPC Code: 8 32007 00110 6
Quantity Affected: 1150 lbs plus expansion 920 lbs
Reason for Recall
May be contaminated with Listeria monocytogenes
Distribution
NY, NJ
Type: Voluntary: Firm initiated
Recall Initiated: 2021-12-21
Company
Jamaica, NY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 153 food recalls issued in the same week, part of 204 food-related FDA actions this month.
D & M Smoked Fish, Inc. has 3 FDA actions in our database, including 3 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (D & M Smoked Fish, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does D & M Smoked Fish, Inc. have FDA actions?
D & M Smoked Fish, Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0505-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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