Home/Recalls/CANADA-77312
Health CanadaType II

Kinesia ONE and Kinesia 360

Published: April 22, 2025Recall ID: 77312Category: generalCountry: Canada

Reason for Recall / Hazard

Unauthorised device

Product Description & Identification

Kinesia ONE and Kinesia 360

Additional Source Details

FieldValue
N I D77312
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/kinesia-one-and-kinesia-360
IssueUnauthorised device
TitleKinesia ONE and Kinesia 360
ProductKinesia ONE and Kinesia 360
Archived0
CategoryNeurology
Last updated2025-04-22
OrganizationMedical devices
Recall classType II

Overview

  • Recalling FirmMedical devices
  • Risk LevelType II
Official Agency Alert