Evis Exera And Evis 140 Video System - Duodenovideoscope (2018-08-14)

Recall Summary Olympus is recalling EVIS EXERA and EVIS 140 video systems with duodenovideoscope models across Canada due to a medical device issue. The recall affects healthcare facilities and medical centers that use these endoscopy systems. This is classified as a Class I recall, which is the most serious classification for medical devices.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-09-07

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/2cd899ba-422c-4f99-91b0-218f73de5c20