Zurion 7 M20, B12 And B20 (2019-12-18)
AZURION 7 M20, B12 and B20 Recall Philips is recalling certain AZURION 7 interventional X-ray systems (models M20, B12, and B20) distributed across Canada due to a potential software issue that could affect device performance. This is a Class I recall, meaning the defect could cause serious injury or death. The recall affects healthcare facilities that use these medical imaging systems.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-01-06
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b25649cc-23c8-418e-a726-51167a5ed0b3