Evis Exera III Duodenovideoscope
Recall Summary The EVIS EXERA III Duodenovideoscope is being recalled across Canada due to labelling and packaging issues. This is a Class I recall, meaning the product could cause serious harm or death. The recall affects all units of this medical device that were distributed in Canada.
- Product
- EVIS EXERA III Duodenovideoscope
- Reason
- Labelling or packaging defect
- Classification
- Class I
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-02-03
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5263a0b2-97d2-4ec7-9f09-3d5518536f6a