FDASeptember 4, 2018device

Leica HistoCore SPECTRA CV Coverslipper, used in preparation of histological and cytological tissue samples for microscopic analysis for medical diagnostics.

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

The hazard

Product was assembled with an isolating fiberglass hose within the oven in the wrong position. This results in improper shielding from potential electrical shock.

What to do

FDA enforcement status: Terminated

Brands named

leica microsystemsleica

Recall history

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

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