Zurion 7 M12, M20 (2019-07-05)
Azurion 7 M12, M20 Recall Summary Philips is recalling Azurion 7 M12 and M20 imaging systems distributed across Canada due to a safety issue with the medical device. The recall affects healthcare facilities that use these X-ray systems. This is a Class I recall, which indicates a serious safety concern.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-07-19
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/89d075e3-c404-4379-b2da-8410290de618