Vanta Implantable Neurostimulator (INS)
Brand(s)
Last updated
Summary
Product
Vanta Implantable Neurostimulator (INS)
Issue
Medical devices - Performance
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 |
|---|---|---|
| Vanta Implantable Neurostimulator (INS) | More than 10 numbers, contact manufacturer. | 977006 |
Issue
The purpose of this recall is to emphasize the impact programming settings can have on the battery life of the Vanta Implantable Neurostimulator (INS) model 977006. Additionally, this letter is intended to remind you of the tools that currently exist in both models A71200 Vanta Clinician Programmer application and A71300 Stimulation Trialing Clinician Programmer application. These tools should be used to assist in selecting the appropriate INS model for the patient and to assess the longevity of the Vanta INS throughout the life of the implant.
Recall start date: August 20, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Neurology
Companies
| Medtronic Inc. |
| 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type I
Identification number
RA-75971
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