Holmium Laser Fiber, Flexor Vue Deflecting Endoscopic System, And Vueoptic Visulation Source (2017-04-24)

Recall Summary Holmium laser fibers and associated endoscopic equipment used in medical procedures are being recalled across Canada due to a defect with the medical devices. This Class I recall affects the Flexor Vue deflecting endoscopic system and Vueoptic visualization source. The recall applies to these devices that were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-06-07
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/72976e1f-7288-43d9-84e6-c5004c42a36f