Zurion 7 M12 And Azurion 7 M20 (2018-03-19)
Azurion 7 M12 and Azurion 7 M20 Recall Philips is recalling Azurion 7 M12 and Azurion 7 M20 medical imaging systems distributed across Canada. The specific reason for the recall has not been detailed in the available information. This is 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
- 2018-05-01
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/0cb55713-06ec-476c-9819-1cb540626b62