Zurion 7 M20 (2020-04-03)
Azurion 7 M20 Recall Summary The Azurion 7 M20 medical device is being recalled across Canada due to a manufacturing issue. This device is used in medical imaging procedures. The recall is classified as Class I, meaning there is a serious potential health risk associated with the device.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-05-01
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d9d3f1dd-0746-4f98-85cd-1894fe918da7