Centrifuge 642 Vfd Plus
Centrifuge 642 VFD Plus Recall Summary The Centrifuge 642 VFD Plus is being recalled in Canada because it is an unauthorized medical device. This device was distributed across Canada and has been classified as a Class I recall, which is the most serious category. Anyone in Canada who possesses this centrifuge should be aware of this recall.
- Product
- Centrifuge 642 VFD Plus
- Reason
- Unauthorised device
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2021-12-07
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b47d0f69-3ba7-4423-a8c0-a44e70f90fe7