Azurion R2.1.10 And R2.2.10 Systems
Recall Summary Philips is recalling Azurion R2.1.10 and R2.2.10 imaging systems in Canada due to a performance issue. This recall affects medical facilities that use these systems. The FDA has classified this as a Class I recall, indicating a serious concern.
- Product
- Azurion R2.1.10 and R2.2.10 systems
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-12-29
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/7956cfa9-f76a-44e7-bb2b-0bd6c00f7e8f