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:
Alert / recall type
Health product recall
Category
Health products - Medical devices - 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
Get notified
Receive notifications for new and updated recalls and alerts by category.