FDAApril 10, 2024device

Leica HistoCore PEGASUS Tissue Processor, REF 14048858005.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Poorly processed and/or damaged biopsy tissue specimens on the device resulting from reagent levels exceeding the maximum fill level marks on reagent bottles or in the paraffin tanks.

What to do

FDA enforcement status: Ongoing

Brands named

leica biosystems nusslochleicaleica biosystems

UPCs

0404918821639714048858005

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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