Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Recalled by Medtronic Neuromodulation Due to The Implantable Neurostimulator Model may be susceptible to...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Neuromodulation directly.
Affected Products
Vanta INS Implantable Neurostimulator. Medtronic Model 977006 Vanta with AdaptiveStim Technology Neurostimulator with Surescan MRI technology, part of a neurostimulator system for pain therapy.
Quantity: 1021 devices
Why Was This Recalled?
The Implantable Neurostimulator Model may be susceptible to not communicating with the clinical programmer and/or patient programmer system.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Neuromodulation
Medtronic Neuromodulation has 95 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report