Verathon, Inc. recalls GlideScope Go Monitors

Recall date

July 1, 2021

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2172-2021

FDA classification

Class III

Brand / firm

Verathon, Inc.

Sold / distributed

U.S.: AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, Guam, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, Puerto Rico, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV and WY. O.U.S.: Australia, Brunei Darussalam, Canada, Czech Republic, Denma…

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.

Class III means the product violates regulations but is not likely to cause harm.

What was recalled

GlideScope Go Monitors