Product Wiki · Recalls · Health Canada — Medical Devices

Kinesia ONE and Kinesia 360 — recall 77312

Health Canada — Medical Devices · Canada · 2025-04-22 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
77312
Date of alert
2025-04-22
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Neurology
Product type
Medical devices
Reported risk: 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
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/kinesia-one-and-kinesia-360

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