Duodenoscope (2020-04-30)

Duodenoscope Recall Summary Duodenoscopes, which are medical devices used to examine the small intestine, have been recalled across Canada. The recall is classified as Class I, meaning there is a serious potential health risk associated with the devices. The devices were distributed nationwide in Canada.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2020-05-29
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/e619c135-e51a-49d7-9dd3-7305432ec648