Philips Achieva, Intera And Ingenia Systems
Philips MRI System Recall Summary Philips Achieva, Intera, and Ingenia magnetic resonance imaging (MRI) systems are being recalled across Canada due to a performance issue. This recall affects medical facilities using these MRI systems. The FDA has classified this as a Class I recall, which is the most serious type.
- Product
- Philips Achieva, Intera and Ingenia Systems
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-01-17
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/a707bb97-21a0-4fa4-875c-584a2862727e