Zurion 7m12, M20, B12 & B20 (2019-11-04)
Azurion 7M12, M20, B12 & B20 Recall Philips is recalling certain Azurion imaging systems (models 7M12, M20, B12, and B20) distributed across Canada due to a potential safety issue with the medical device. This is a Class I recall, which indicates a serious health hazard. The recall affects healthcare facilities that have these imaging systems in use.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-11-15
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/ddf19f4e-3891-48a6-8d2b-14fa32b2e975