Buckhead Tuna
Reason The Firm was notified by NJ Department of Health of two samples collected from tuna with reported high levels of scombrotoxin.
Foppen Smoked Norwegian Salmon Slices recall
Recalled by Foppen Paling En Zalm B.V. · Harderwijk, Netherlands
Class I — High risk. Reasonable probability of serious harm or death.
Why it was recalled
Potential contamination with 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
Foppen Smoked Norwegian Salmon Slices - Toast Size, packaged in 8.1oz vacuum foil, packaged within cardboard envelope. Keep Refrigerated at 38F or below.
Quantity: 747 cases
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.
Batch No 1205412 Lot 412 printed on pack, 1205412 printed on case Product No 850094
Where it was sold
Alabama Arkansas Georgia Illinois Indiana Kentucky Louisiana Michigan Missouri Mississippi Ohio South Carolina Tennessee Texas West Virginia
FDA's distribution note: AL, AR, GA, IL, IN, KY, LA, MI, MO, MS, OH, SC, TN, TX and WV
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
- Foppen Paling En Zalm B.V.
- Initiated by
- Voluntary: Firm initiated
- Recall initiated
- Jun 21, 2024
- In FDA report of
- Aug 21, 2024
- Terminated
- Aug 13, 2024
- FDA recall number
- F-1728-2024 · event 94883
- Official record
- FDA enforcement report search
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