Recall

Class I — Verathon, Inc.

Recalling firm	Verathon Inc.
Registered facility	Verathon Inc. (the firm's only registered facility)
Classification	Class I
Status	Terminated
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.
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.
Quantity	437
Distribution	Worldwide Distribution: US (nationwide) and countries of: Australia and United Kingdom.
Initiated	2020-06-05
Classified	2020-07-09
Terminated	2024-04-22
Recall number	Z-2476-2020
Initiation	Voluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class I recall — Verathon, Inc. (Z-2476-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85705/

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