Verathon, Inc. recalls GlideScope Go Monitors

Recalled August 11, 2021 · FDA recall Z-2172-2021 · Verathon

Hazard

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

Units

8,569

Sold at

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, Denmark, Estonia, Falkland Island (Malvinas), France, Germany, Greece, Hong Kong, Iceland, Ireland, Israel, Italy, Kuwait, Luxembourg, Malaysia, New Zealand, Oman, Papua New Guinea, Philippines, Portugal, Qatar, Reunion, Romania, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, Thailand, The Netherlands, United Arab Emerita, and United Kingdom.

Description

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

Product

GlideScope Go Monitors

Manufacturer(s)

Verathon, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →