Versapulse Dual Wavelength And Co2 Laser Systems

VersaPulse Dual Wavelength and CO2 Laser Systems are being recalled across Canada due to a labeling or packaging defect. These medical laser devices are affected by this Class II recall. The issue involves problems with how the products are labeled or packaged.

Product
VersaPulse Dual Wavelength and CO2 Laser Systems
Reason
Labelling or packaging defect
Classification
Class II
Category
medical device recall
Country
Canada
Agency
HC-DEVICES
Recall date
2026-05-13
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/6d02cc0c-186c-4367-8467-05b4a8778f67