Fred® Flow Re-direction Endoluminal Device
Recall Summary The Fred® Flow Re-Direction Endoluminal Device is being recalled in Canada due to performance concerns. This device is used in medical procedures inside blood vessels. The recall affects all units distributed across Canada.
- Product
- Fred® Flow Re-Direction Endoluminal Device
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-11-04
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/91e14cbe-6722-43e9-a744-582bf6d797e1