Quick summary
Quick summary: Elite Centrifuge.
Public recall detail
Elite Centrifuge
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: Elite Centrifuge.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandElitemed Inc
ProductElite Centrifuge
IssueMedical devices - Unauthorised device
Recall classType II
IdentificationRA-63687
Affected products
ProductElite Centrifuge
LotAll lots.
ModelDM0412
Serial numberAll lots.
DescriptionElite Centrifuge
Issue
The centrifuge is advertised with a PRP indication which classifies it as a class II medical device in Canada. The Elite Centrifuge does not have a class II licence, and therefore is not authorized for sale in Canada. Recall start date: Nov 29, 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
CompaniesElitemed Inc 3190 Ridgeway Drive, Mississauga, Ontario Canada, L5L 5S8
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-63687
Background{}
CompaniesElitemed Inc 3190 Ridgeway Drive, Mississauga, Ontario Canada, L5L 5S8
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.
FAQ
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Product images
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