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# Verathon Recalls GlideScope Video Cable
- URL: https://www.fdaweb.com/verathon-recalls-glidescope-video-cable/
- Published: 2020-07-17T12:00:00.000Z
- Updated: 2026-09-14T16:21:38.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5147223

Verathon has recalled the GlideScope Core One TouchSmart Cable, which is part of its Video Laryngoscopy System, due to the potential for temporary or complete loss of image when used with Core 10 and Core 15 video monitors. “If there is an interruption in the video signal during use, this may cause the patient to experience serious adverse health consequences, including hypoxia and death,” a recall notice says. Verathon says it has received 74 complaints and the agency has received nine Medical Device Reports associated with the problem. The Video Laryngoscopy System is intended to provide a clear view of the airway and vocal cords for medical procedures.