FDA recall record

Leica HistoCore PEGASUS recall — FDA Z-0590-2024

There is an issue regarding poorly processed and/or damaged biopsy tissue specimens on the HistoCore PEGASUS / HistoCore PEGASUS Plus resulting from an…

Class IIclassification
Z-0590-2024official record ID
May 1, 2024report date

Recall record at a glance

Official recordZ-0590-2024
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmLEICA BIOSYSTEMS NUSSLOCH GMBH
Report dateMay 1, 2024
Recall initiation dateNov 20, 2023
Quantity98 devices
LocationNussloch, N/A, Germany

Official product description

Leica HistoCore PEGASUS (PROCESSOR, TISSUE, AUTOMATED)

Why the product was recalled

There is an issue regarding poorly processed and/or damaged biopsy tissue specimens on the HistoCore PEGASUS / HistoCore PEGASUS Plus resulting from an incorrect assignment of the carryover value set for created or edited protocols.

Distribution information

US, Nationwide

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: 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

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