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Health Canada Medical devices

Centrifuge 642 VFD Plus

Issued December 7, 2021
Issue
The manufacturer distributed the centrifuges 642 VFD plus in canada contain PRP references in the manual, front panel and on the device labeling. The Canadian authorities indicated that the issue needs to be revised for a class I standard. Recall start date: Dec 25, 2021
Hazard description
Unauthorised device
Product
Product name
Centrifuge 642 VFD Plus
Reference
ID
RA-63691