SMOKED NOVA Salmon
Reason Virginia Department of Agriculture and Consumer Services revealed the presence of Listeria monocytogenes in Smoked Nova Salmon.
KIRKLAND Signature Smoked Salmon recall
Recalled by Acme Smoked Fish Corp. · Brooklyn, NY, United States
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
The firm was notified after laboratory analysis that the product test positive for Listeria monocytogenes.
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
KIRKLAND Signature Smoked Salmon NET WT 340 g (12 oz) MUST KEEP REFRIGERATED. INGREDIENTS: Atlantic Salmon (Salmo Salar), Salt, and Natural Hardwood Smoke. Color Added. Distributed by: Costco Wholesale Corporation P.O. Box 34535 Seattle, WA 98124-1535 UPC 0 96619 25697 6
Quantity: 111cs/16/2/12oz packs
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 8512801270 Best By 11/13/2024
Where it was sold
Florida
FDA's distribution note: Product was shipped to distribution center and retail stores in FL
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
- Acme Smoked Fish Corp.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Oct 22, 2024
- In FDA report of
- Jan 29, 2025
- Terminated
- Jan 13, 2026
- FDA recall number
- F-0420-2025 · event 95612
- Official record
- FDA enforcement report search
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