FDA recall record

Foppen Paling En Zalm B.V packaged in 8.1oz vacuum foil, packaged within cardboard recall — FDA F-1728-2024

Potential contamination with Listeria monocytogenes

Class Iclassification
F-1728-2024official record ID
Aug 21, 2024report date

Recall record at a glance

Official recordF-1728-2024
CategoryFood Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmFoppen Paling En Zalm B.V.
Report dateAug 21, 2024
Recall initiation dateJun 21, 2024
Quantity747 cases
LocationHarderwijk, Netherlands

Official product description

Foppen Smoked Norwegian Salmon Slices - Toast Size, packaged in 8.1oz vacuum foil, packaged within cardboard envelope. Keep Refrigerated at 38F or below.

Why the product was recalled

Potential contamination with Listeria monocytogenes

Distribution information

AL, AR, GA, IL, IN, KY, LA, MI, MO, MS, OH, SC, TN, TX and WV

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.