Reported Jul 15, 2020 · Terminated
GlideScope Core OneTouch Smart Cable, REF: 0800 0601, an accessory to the GlideScope Video Laryngoscope System Per…
Verathon, Inc.
High riskUsing this product could cause serious injury, illness or death — stop using it now.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Verathon, Inc. · 20001 N Creek Pkwy · Bothell, WA · 98011-8218
Is this the product you have?
- GlideScope Core OneTouch Smart Cable
- REF0800 0601, an accessory to the GlideScope
- Video Laryngoscope System Per PLRAThe 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
- Lot codes and dates
- All serial numbers
- Amount recalled
- 437
Where it was sold
- Nationwide
Why it was recalled
Stop using this product now
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.
Using this product could cause serious injury, illness or death — stop using it now.
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