Overview of recall records associated with Verathon, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 4, Class III: 1, Class I: 1.
Due to software issues, their is the potential for loss of image or a degradation of the image when using the monitor with other connectable devices.
Due to software issues, their is the potential for loss of image or a degradation of the image when using the monitor with other connectable devices.
Handheld video monitor failed to meet the labeled IP67 rating which may allow fluid ingress into the monitor resulting in loss of functionality.
Due to a change in handle material and process, probe handle may crack.
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…
A typographical error in the Operations & Maintenance Manual incorrectly identifies the use of low level disinfection for the reusable video laryngoscope, specifically for the Titanium…
This page summarizes recall records in which the official source identifies Verathon, Inc. as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.
