Kinesia One And Kinesia 360

Kinesia ONE and Kinesia 360 devices have been recalled across Canada because they are unauthorized medical devices. These products were not approved by Health Canada before being sold. This recall affects all consumers who purchased these devices in Canada.

Product
Kinesia ONE and Kinesia 360
Reason
Unauthorised device
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2025-04-22
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d5af98b9-931a-4722-84f1-55b0bfb0d0f1