Sliced Smoked ATLANTIC SALMON
Reason Environmental samples collected by the Food and Drug Administration revealed the presence of Listeria monocytogenes which has the potential to contaminate food products.
ATLANTIC Smoked SALMON Whole recall
Recalled by K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd. · Mount Kisco, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Environmental samples collected by the Food and Drug Administration revealed the presence of Listeria monocytogenes which has the potential to contaminate food products.
Pathogen: Listeria
Listeria monocytogenes can grow even in the fridge and is especially dangerous in pregnancy.
The most serious food recalls: a contaminated product can cause outbreaks, hospitalisations and deaths, especially for pregnant people, young children, older adults and anyone with a weakened immune system. All bacteria & viruses recalls.
What was recalled
ATLANTIC Smoked SALMON Whole, Net Wt. 8 OZ (225.89), Keep Refrigerated 38¿F or Below
Quantity: 158 units
Food: Seafood & fish
Lot codes, dates and UPCs
A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.
lot # 13723516 USE BY 09 12 16 lot # 12125316 USE BY 09 30 16
Where it was sold
Connecticut New York
FDA's distribution note: CT & NY via retail stores
Do not eat it. Class I means FDA judged there is a reasonable probability of serious illness or death. If the brand, size and lot or date code on your package match, throw the product away or return it to the store for a refund, and clean any surface or container it touched. If anyone has eaten it and feels unwell, contact a doctor and mention the recall. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.
- Recalling firm
- K & P Marketplace Ltd. d.b.a Mt. Kisco Smokehouse Ltd.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Sep 26, 2016
- In FDA report of
- Oct 26, 2016
- Terminated
- May 8, 2017
- FDA recall number
- F-0211-2017 · event 75264
- Official record
- FDA enforcement report search
Also recalled with it (1 more product)
FDA files each product of one recall action separately; these share the same FDA event.
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