Recall Z-2172-2021— Verathon, Inc.

Name: FDA recall Z-2172-2021
Creator: U.S. Food and Drug Administration
Published: 2021-07-01

Class III · Ongoing

Class III FDA medical device recall by Verathon, Inc., initiated 2021-07-01. FDA's recall record names no specific 510(k) clearance for this event. Product: GlideScope Go Monitors. Reason: Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality..

Recalling firm: Verathon, Inc.
Classification: Class III
Status: Ongoing
Initiated: 2021-07-01
Firm location: Bothell, WA, United States

Product description

GlideScope Go Monitors

Reason for recall

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

Data sourced from openFDA. This site is unofficial and independent of the FDA.