Recall MonitorHealth Products
Kinesia ONE and Kinesia 360
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Neurology
Product: Kinesia ONE and Kinesia 360
Issue: Medical devices - Unauthorised device
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
Products
| Affected products | Lot or serial number | Model or catalog number |
|---|---|---|
| Kinesia ONE | Not applicable. | 700-0019 |
| Kinesia 360 | Not applicable. | 700-0020 |
Issue
The Kinesia ONE and Kinesia 360 products are being recalled because they were incorrectly sold as class I devices but should have been classified as class II devices, and thus do not have valid Medical Device Licenses (MDL). Recall Start Date: March 28, 2025