Reported Aug 11, 2021 · Ongoing

GlideScope Go Monitors

Verathon, Inc.

Low riskThis product is unlikely to cause harm, but it breaks a safety or labelling rule.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Verathon, Inc. · 20001 N Creek Pkwy · Bothell, WA · 98011-8218

Is this the product you have?

  • GlideScope Go Monitors
Lot codes and dates

2,957 of 2,957 products

Products covered by this recall
Model / numberProduct as published
0570-0366Software Version: v.1.4 Serial Numbers: 1450070 HM082506
—HM171547
—HM171548
—HM171550
—HM171622
—HM171627
—HM171629
—HM171630
—HM171631
—HM171632
—HM171633
—HM171634
—HM171635
—HM171636
—HM171637
—HM171638
—HM171639
—HM171642
—HM171643
—HM171644
Amount recalled
8,569

Where it was sold

Why it was recalled

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

This product is unlikely to cause harm, but it breaks a safety or labelling rule.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Nov 4, 9:36 AM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.