Medtronic Stent Graft Systems (2019-02-10)
Medtronic Stent Graft Systems Recall Medtronic is recalling certain stent graft systems used to treat aortic aneurysms and other blood vessel conditions. The recall was issued due to concerns with the medical device itself. This recall affects stent graft systems distributed across Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-02-22
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/113bb5d2-120e-45bf-8253-19a92ea74810