Allura Xper And Azurion 7
Recall Summary Philips is recalling ALLURA XPER and AZURION 7 medical imaging systems across Canada due to a software defect. These are X-ray imaging devices used in hospitals and medical facilities. The recall is classified as Class I, meaning the defect could cause serious injury or death.
- Product
- ALLURA XPER and AZURION 7
- Reason
- Software defect
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2021-11-12
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/4b267c45-df05-4255-8544-87ff43ddaa13