Achieva 3.0t Mri System-main Unit
Recall Summary Philips is recalling Achieva 3.0T MRI System-Main Unit devices distributed across Canada due to a performance issue. This is a Class I recall, which indicates a serious problem with the device. The recall affects MRI systems that were distributed throughout Canada.
- Product
- Achieva 3.0T MRI System-Main Unit
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-12-18
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b39fe0ca-7692-4aaa-ba42-17484567b351