FDA Device recall Z-2476-2020
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
- terminated
- Published 2020-07-15
On 2020-07-15 the FDA classified a Class I recall of GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per PLRA: The Core OneTouch… by Verathon, citing when video laryngoscopy system users apply, twisting motions while connecting the blade in the HDMI port, or excessive torsion to the connection port, this force is transferred to….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2476-2020 |
| Classification | Class I |
| Status | terminated |
| Initiated | 2020-06-05 |
| Published | 2020-07-15 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Verathon |
| Distribution | US |
Product
GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per PLRA: The Core OneTouch Cables (Reusable Device) is ancillary equipment used with the Core 10 and Core 15 monitors. The monitor and workstation are intended to work with video endoscopes, in conjunction with ancillary equipment, for endoscopic procedures.
Reason
When video laryngoscopy system users apply, twisting motions while connecting the blade in the HDMI port, or excessive torsion to the connection port, this force is transferred to the HDMI PCB, which may result in video synchronization interruption, loss of live image/blank screen, no cameras connected monitor warning, may present risk to patients, in which time to intubation is more critical.
Identifiers
| code_info | All serial numbers |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
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 - GlideScope Go Monitors
FDA Device · Class III · 2021-08-11 · 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 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-2476-2020%22
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