Product Wiki · Recalls · Health Canada — Medical Devices

Myndmove Functional Electrical Stimulater — recall 56296

Health Canada — Medical Devices · Canada · 2017-03-10 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
56296
Date of alert
2017-03-10
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: To upgrade affected products with corrections to hardware, software and mechanical components. The corrections are improvements to address software bugs and usability issues identified with the product through Myndtec's complaint handling procedure. The recall does not affect the products safety, benefits or effectiveness.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/myndmove-functional-electrical

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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