FDAJune 5, 2020device

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 endosc...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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.

What to do

FDA enforcement status: Terminated

Brands named

verathon

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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