Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
GlideScope Core OneTouch Smart Cable Recalled by Verathon, Inc. Due to When video laryngoscopy system users apply, twisting motions...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Verathon, Inc. directly.
Affected Products
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
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Verathon, Inc.
Verathon, Inc. has 13 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report