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FDAJuly 1, 2021device

GlideScope Go Monitors

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

The hazard

Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality.

What to do

FDA enforcement status: Ongoing

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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GlideScope Go Monitors — Recall Details · AllClear