Optilite Holmium Fiber Assembly And Lser Fibers (2017-06-13)

Recall Summary Optilite Holmium Fiber Assembly and Laser Fibers are being recalled across Canada due to a medical device issue. This affects holmium laser fiber products distributed in Canada. The FDA classified this as a Class I recall, indicating a serious safety concern.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-07-07

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/f23266f2-0c46-4560-b44c-209be91a09aa