Polestar N-20 - Magnetic Resonance Diagnostic Device (2016-06-28)
Polestar N-20 Recall Summary The Polestar N-20 magnetic resonance diagnostic device is being recalled across Canada due to a medical device issue classified as Class I, the most serious type. The recall affects all units of this diagnostic imaging device that were distributed in Canada. No further details about the specific defect or affected patient populations are provided in this notice.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-08-05
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/c63ea3d2-b2ec-41ea-9b5f-115c13a3cc17