Evis Exera III Duodenovideoscope
Recall Summary Pentax Medical is recalling Evis Exera III Duodenovideoscope devices across Canada because they may not be sterile. This is a Class I recall, meaning there is a serious potential for harm. The affected devices were distributed throughout Canada.
- Product
- Evis Exera III Duodenovideoscope
- Reason
- Sterility
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-10-10
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/19152aaa-692d-4535-9141-bc2336a6887d