Health product recall

Elite Centrifuge

Brand(s)
Last updated

Summary

Product
Elite Centrifuge
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

Elite Centrifuge

All lots.

DM0412

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

Additional information

Details
Original published date: 2021-12-10
Alert / recall type
Health product recall
Category
Health product - Medical device
Companies
Elitemed Inc

3190 Ridgeway Drive, Mississauga, Ontario

Canada, L5L 5S8

Published by
Health Canada
Audience
General public
Health professionals
Hospitals
Recall class
Type II
Identification number
RA-63687