Flexible Intubation Endoscopes (2020-07-27)

Flexible Intubation Endoscopes Recall Flexible intubation endoscopes are being recalled across Canada due to a medical device issue. This recall is classified as Class I, meaning there is a serious potential health risk. The affected devices were distributed throughout Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-08-28
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/85bec47a-7286-4824-b6b8-4717338e1abf