Activa Clinician Programmer Application For Deep Brain Stimulation

Recall Summary The Activa Clinician Programmer Application, software used to program deep brain stimulation devices, is being recalled across Canada due to device compatibility issues. The recall is classified as Class I, meaning there is a reasonable possibility that use of the product could cause serious injury or death. The software affects deep brain stimulation systems used by clinicians to adjust patient treatment settings.

Product
Activa Clinician Programmer Application For Deep Brain Stimulation
Reason
Device compatibility
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2022-08-02
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/bc4790e3-c818-42b7-9fbc-a70b0290102f