Verathon, Inc.: Medical Device Recall in 2020 - (Recall #: Z-2476-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class I

Date Initiated: June 5, 2020

Date Posted: July 15, 2020

Recall Number: Z-2476-2020

Event ID: 85705

Reason for Recall:

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.

Status: Terminated

Product Quantity: 437

Code Information:

All serial numbers

Distribution Pattern:

Worldwide Distribution: US (nationwide) and countries of: Australia and United Kingdom.

Voluntary or Mandated:

Voluntary: Firm initiated