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 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Other recalls by Verathon
- Brand Name: GlideScope Core 15-inch FHD Model/Catalog Number: 0570-0437 Software Version: Core 15 FHD v1.7 and earlier Product Description:…
FDA Device · Class II · 2024-06-12 · Verathon - Brand Name: GlideScope Core 15-inch Monitor Model/Catalog Number: 0570-0404 Product Description: Serialized Monitor
FDA Device · Class II · 2024-06-12 · Verathon - BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the bladder noninvasively
FDA Device · Class II · 2020-12-09 · Verathon - GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per PLRA: The Core OneTouch…
FDA Device · Class I · 2020-07-15 · Verathon - GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
FDA Device · Class II · 2020-03-18 · Verathon
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2172-2021%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.