Quick summary
Quick summary: Centrifuge 642 VFD Plus.
Public recall detail
Centrifuge 642 VFD Plus
Recall
Safety notice
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: Centrifuge 642 VFD Plus.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandDrucker Diagnostics
ProductCentrifuge 642 VFD Plus
IssueMedical devices - Unauthorised device
Recall classType II
IdentificationRA-63691
Affected products
ProductCentrifuge 642 Vfd Plus
LotAll lots.
Model00-027-088-003
Serial numberAll lots.
DescriptionCentrifuge 642 Vfd Plus
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
What you should do
- Contact the manufacturer if you require additional information.
Additional official information
AudienceGeneral public Health professionals Hospitals
CategoryHealth products - Medical devices
CompaniesDrucker Diagnostics 200 Shadylane Drive, Philipsburg, Pennsylvania United States, 16866
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-63691
Background{}
CompaniesDrucker Diagnostics 200 Shadylane Drive, Philipsburg, Pennsylvania United States, 16866
AudiencesGeneral public Health professionals Hospitals
Source updated2021-12-07
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
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