Official recall record
Kinesia ONE and Kinesia 360
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-04-22
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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