FDAJune 13, 2018device

Leica Biosystems HistoCore SPECTRA ST, Slide Stainer, Automated Product Usage: The intended use of this device is a stainer for laboratory applications and intended for the preparation of histological and cytological specimens.

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

The hazard

These devices have an incorrect specification against safety standard ISO61010-1. Should a single fault error occur, a mains wire can contact a metal plate which is accessible to the user. This could lead to mains power on the metal plate resulting in hazardous voltage to the user.

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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Leica Biosystems HistoCore SPECTRA ST, Slide Stainer, Automated Product Usage: The intended use of this device is a stainer for laboratory applications and intended for the preparation of histological and cytological specimens. — Recall Details · AllClear