Every recall we track for Verathon, Inc. — 6 in all — plus the complaints and injury reports the public filed about them.
Verathon recalls GlideScope Core 15-inch monitors (model 0570-0404) with software v1.9 or earlier due to potential image loss when connected to other devices. Affected units may need software update.
Verathon recalls GlideScope Core 15-inch FHD monitors with software v1.7 and earlier due to potential image loss or degradation when connected to other devices. Affected units may require software updates to prevent issues.
Verathon recalls GlideScope Go Monitors with specific serial numbers and software versions for potential fluid ingress due to failed IP67 rating, which could cause loss of functionality.
Verathon recalls BladderScan Prime Plus Probe REF 0570-0395 due to handle cracking risk. Affected units have specific serial numbers listed. Stop using if handle cracks.
Verathon recalls GlideScope Core OneTouch Smart Cable (REF 0800 0601) due to potential video disruption during intubation, risking critical patient delays. Affected users should check serial numbers and contact Verathon for details.
Verathon recalls GlideScope Video Laryngoscope manual with incorrect low-level disinfection instructions for titanium blades. Affected units include specific revisions and serial numbers. Contact for correction.