Evis Exera Video System - Duodenovideoscopes (2016-04-18)

Recall Summary Olympus is recalling EVIS EXERA video duodenoscopes (medical scopes used to examine the small intestine) distributed across Canada due to safety concerns with the device. The recall is classified as Class I, meaning there is a reasonable probability that use of the product will cause serious adverse health consequences or death. This recall affects medical facilities that use these specific duodenoscope models.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2016-04-29
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/a79e141a-8476-435e-9892-10221972d0e7