FDAMarch 31, 2019device

GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03

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

The hazard

A typographical error in the Operations & Maintenance Manual incorrectly identifies the use of low level disinfection for the reusable video laryngoscope, specifically for the Titanium Blades.

What to do

FDA enforcement status: Terminated

Brands named

verathon

Recall history

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

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