Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Model A710 Intellis Clinician Programmer Application Recalled by Medtronic Neuromodulation Due to Medtronic has discovered an instance in which the...
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
Model A710 Intellis Clinician Programmer Application, version 2.0.97
Quantity: 1 tablet
Why Was This Recalled?
Medtronic has discovered an instance in which the Intellis A710 Clinician Programmer Application (CP App) could no longer establish a session with the Implantable Neurostimulator (INS) which resulted in the inability for the clinician to adjust stimulation parameters. In the event of this issue, the patient may receive inadequate or excessive therapy and experience non-optimal pain relief.
Where Was This Sold?
Germany
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