Medilas D Laser System - Optical Fiber, Laser Fiber Light Guides (2019-04-27)

Medilas D Laser System Recall Summary Medilas D Laser System optical fibers and laser fiber light guides are being recalled in Canada because they are medical devices that do not meet required safety or performance standards. This recall affects Medilas D Laser Systems distributed across Canada. The FDA classified this as a Class I recall, indicating a serious issue.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2019-06-14

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e4d09c2c-c14b-4da2-b7fc-36ede17efdca