Philips Ingenia
Philips Ingenia Recall Summary Philips Ingenia MRI systems are being recalled in Canada due to performance issues. This recall affects medical facilities across Canada that use this imaging equipment. The FDA has classified this as a Class I recall, the most serious category.
- Product
- Philips Ingenia
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-05-17
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/fb70e69f-aa7b-4caa-877b-bf7337f6d9b6