Angioguard™ Rx Emboli Capture Guidewire System
ANGIOGUARD™ RX Emboli Capture Guidewire System Recall The ANGIOGUARD™ RX Emboli Capture Guidewire System is being recalled across Canada because it is not performing as intended. This is a Class I recall, which means the product could cause serious health problems or death. The recall affects all units of this medical device that were distributed in Canada.
- Product
- ANGIOGUARD™ RX Emboli Capture Guidewire System
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2023-03-28
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/c1969e87-2acc-46fb-a0e4-d66f0e8ee778