Duodenovideoscope
Recall Summary Pentax of Canada is recalling Duodenovideoscopes (medical devices used to examine the small intestine) across Canada due to performance issues. This recall affects healthcare facilities that use these devices. The FDA classified this as a Class I recall, the most serious category.
- Product
- Duodenovideoscope
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2021-12-02
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a23baee6-5af3-48c3-8662-c8cfbf52d139