Azurion And Allura Xper Systems
Recall Summary Philips is recalling Azurion and Allura Xper Systems in Canada due to a device performance issue. These are medical imaging systems used in hospitals and healthcare facilities. The recall is classified as Class II, meaning the issue could cause temporary or medically reversible adverse health effects.
- Product
- Azurion and Allura Xper Systems
- Reason
- Device performance issue
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-05-06
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5efac84b-365b-4275-aaf5-c59cc10df62d