Verathon recalls GlideScope Core OneTouch Smart Cable (REF 0800 0601) due to potential video disruption during intubation, risking critical patient delays. Affected users should check serial numbers and contact Verathon for details.
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.
Verathon recalls the GlideScope Core OneTouch Smart Cable (REF 0800 0601) because improper use can cause video interruptions during intubation, potentially delaying critical patient care. This affects medical professionals using the device for endoscopic procedures.
Twisting the cable while connecting it to the HDMI port or applying excessive force can cause video synchronization issues. This may lead to a blank screen or loss of live video, delaying critical intubation procedures and increasing patient risk.
Medical professionals using the GlideScope Video Laryngoscope System with this cable for intubation procedures are most at risk. Patients undergoing endoscopic procedures may face delays if the video feed is interrupted.
Check the product's serial number on the cable. This cable is part of the GlideScope Video Laryngoscope System and is sold with the Core 10 or Core 15 monitors.
Look for the serial number on the GlideScope Core OneTouch Smart Cable to confirm if it's affected.
No, the hazard only occurs with improper use, such as twisting the cable while connecting it to the HDMI port.
Check the serial number on the cable; this specific model (REF 0800 0601) is part of the GlideScope Video Laryngoscope System.
The recall record does not specify a remedy, so contact Verathon directly for further instructions.
We’ve drafted a message you can send Verathon to request your refund or repair — edit it as you like.
Subject: Recall Z-2476-2020 — Verathon Verathon Hello, I own a Verathon that is covered by recall Z-2476-2020 from Verathon. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
