Vanguard Knee System Femoral Augment (2016-08-12)
Vanguard Knee System Femoral Augment Recall Vanguard Knee System Femoral Augment knee implant components are being recalled in Canada due to a manufacturing defect. The recall affects patients who received this implant across Canada. This is a Class I recall, meaning the defect could cause serious injury or death.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-08-19
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/8761cd1f-83c2-4f68-b39d-4b51e841631b