Medtronic Neuromodulation recalls Medtronic Intellis Spinal Cord Stimulator, Model Number A710
Recalled Product
Medtronic Intellis Spinal Cord Stimulator, Model Number A710, Clinical Programmer application version 1.3.80 - Product Usage: intended for use by clinicians in the programming of the following Medtronic neurostimulators (external and implantable) for pain therapy.
Hazard / Issue
A710 Intellis Clinician Application has a software issue that can result in the inability to program the Intellis implantable neurostimulation device.
Issued by
FDA
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