FDA Device recall Z-2172-2021
GlideScope Go Monitors
- FDA Device
- Class III
- ongoing
- Published 2021-08-11
On 2021-08-11 the FDA classified a Class III recall of GlideScope Go Monitors by Verathon, citing handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2172-2021 |
| Classification | Class III |
| Status | ongoing |
| Initiated | 2021-07-01 |
| Published | 2021-08-11 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Verathon |
| Distribution | AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, 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, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA, WI, WV, WY |
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.
Identifiers
| code_info | Part Number: 0570-0366 Software Version: v.1.4 Serial Numbers: 1450070 HM082506; HM171547; HM171548; HM171550;…Part Number: 0570-0366 Software 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; HM171645; HM171653; HM171654; HM171655; HM171678; HM171683; HM171685; HM171687; HM171688; HM171689; HM171690; HM171691; HM171692; HM171693; HM171695; HM171707; HM171709; HM171747; HM171748; HM171749; HM171750; HM171751; HM171752; HM171753; HM171754; HM171755; HM171758; HM171759; HM171760; HM171761; HM171763; HM171764; HM171794; HM171799; HM171800; HM171801; HM171802; HM171803; HM171804; HM171806; HM171807; HM171808; HM171809; HM171810; HM171811; HM171812; HM171813; HM171814; HM171815; HM171816; HM171817; HM171819; HM171820; HM171821; HM171822; HM171823; HM171824; HM171825; HM171826; HM171827; HM171828; HM171829; HM171830; HM171832; H |
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Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2172-2021%22
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