Rtis (2020-12-03)
ARTIS Recall Summary ARTIS medical devices are being recalled across Canada due to safety or effectiveness concerns classified as Class I, which indicates a serious potential health risk. The recall affects all ARTIS devices distributed in Canada as of December 3, 2020. Consumers who have this device should check official Health Canada or product documentation for specific next steps.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-12-24
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/e724316c-a08b-47f9-8d63-1d0ff3361169