Centrifuge 642 VFD Plus
Brand(s)
Last updated
Summary
Product
Centrifuge 642 VFD Plus
Issue
Medical devices - Unauthorised device
What to do
Contact the manufacturer if you require additional information.
Affected products
Affected Products |
Lot or serial number |
Model or catalog number |
|---|---|---|
Centrifuge 642 Vfd Plus |
All lots. |
00-027-088-003 |
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
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices
Companies
| Drucker Diagnostics |
|
200 Shadylane Drive, Philipsburg, Pennsylvania United States, 16866 |
Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-63691
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