Azurion 7 M20
Recall Summary Philips Medical Systems Nederland B.V. is recalling the Azurion 7 M20 device across Canada due to a device performance issue. This is a Class II recall, meaning the device could cause serious adverse health consequences but is not likely to cause death. The recall affects all Azurion 7 M20 devices distributed in Canada.
- Recalling firm
- Philips Medical Systems Nederland B.V.
- Product
- Azurion 7 M20
- Reason
- Device performance issue
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-11-13
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/7a9952c7-e290-4032-a1bd-9edb0c579e89