Health product recall

Activa Clinician Programmer Application For Deep Brain Stimulation

Brand(s)
Last updated

Summary

Product
Activa Clinician Programmer Application For Deep Brain Stimulation
Issue
Medical devices - Device compatibility
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalogue number

Activa Clinician Programmer Application For Deep Brain Stimulation

More than 10 numbers, contact manufacturer.

A610

Issue

A system error and termination of program may occur. This may occur when a patient was previously programmed with an A610 dbs clinician programmer application v.2.0.x or later, and later the same device is interrogated with a clinical programmer tablet running A610 version 3.0. 1062.

Recall start date: July 26, 2022

Additional information

Details
Original published date: 2022-08-05
Alert / recall type
Health product recall
Category
Health product - Medical device - General hospital and personal use
Companies

Medtronic Inc.

8200 Coral Sea Street N.E., Mounds View, Minnesota, United States, 55112

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-64430