Discovery Mr750w 3.0t Magnetic Resonance Imaging System (2016-06-09)
Recall Summary GE Healthcare's Discovery MR750W 3.0T magnetic resonance imaging (MRI) system has been recalled across Canada due to a safety issue with the medical device. The recall affects MRI systems distributed in Canada since the device's introduction. This is classified as a Class I recall, indicating a serious potential health hazard.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-06-30
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/6e001529-cc71-4b0d-bff4-fff0067626c7