FDA recall record

Leica HistoCore Arcadia H, REF: 14039354100 and 14039357258, Paraffin Embedding Station recall — FDA Z-2529-2024

An issue with safe usage of the device was identified whereby toxic smoke and internal fire developed resulting from a problem associated with the sealing…

Class IIclassification
Z-2529-2024official record ID
Aug 14, 2024report date

Recall record at a glance

Official recordZ-2529-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmLEICA BIOSYSTEMS NUSSLOCH GMBH
Report dateAug 14, 2024
Recall initiation dateMay 10, 2024
Quantity180 devices
LocationNussloch, Germany

Official product description

Leica HistoCore Arcadia H, REF: 14039354100 and 14039357258, Paraffin Embedding Station.

Why the product was recalled

An issue with safe usage of the device was identified whereby toxic smoke and internal fire developed resulting from a problem associated with the sealing of the paraffin tank.

Distribution information

US Nationwide, including government distribution.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

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.

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