Recall Z-2476-2020

Verathon, Inc. · initiated June 5, 2020

Class I Terminated

Class I – dangerous or defective products that could cause serious health problems or death

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.

Codes / lots: All serial numbers

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.

FDA-determined cause: Device Design

Action taken

On 06/05/20, Field Safety Notice/ URGENT:MEDICAL DEVICE RECALL notices were sent to customers. Customers were asked to do the following: - Review the information contained within this Field Safety Notice with all staff members who should be aware of the contents of the Field Safety Notice. - Discontinue use of all affected cables. - When replacements are received, destroy or return all affected cables in your possession. - Complete and return the recall response form. Customers with additional questions are encouraged to contact Customer Care agent support Monday through Friday from 6:00am to 4:00pm Pacific Time for the United States at (800) 331-2313 or email CSNotifications@verathon.com

Details

Recall number
Z-2476-2020
Initiated
June 5, 2020
Posted by FDA
July 10, 2020
Terminated
April 22, 2024
Product code
CCW – Laryngoscope, Rigid
Quantity
437
Distribution
Worldwide Distribution: US (nationwide) and countries of: Australia and United Kingdom.
Recalling firm
Verathon, Inc., Bothell, WA

Official FDA recall record