Verathon, Inc.: Medical Device Recalls in 2020

According to to data from the FDA, there were 3 medical device recalls made by Verathon, Inc. in 2020. See the details of the recalls below.

You can see similar recalls for other firms.

• GlideScope Video Laryngoscope, Operations & Maintenance Manual, 0900-4940 REV 03
• 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.
• BladderScan Prime Plus Probe REF 0570-0395 - Product Usage: intended to be used for measuring the urine volume in the bladder noninvasively.