Medtronic Neuromodulation Recall 86872
Description: 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.
Medtronic Neuromodulation Recall 86872 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-0860-2021 |
| Event ID | 86872 |
| Event Description | 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. |
| Product Type | Devices |
| Distribution | Worldwide distribution - US Nationwide distribution and the countries of Canada, Latin America, Asia Pacific, Japan, China, and European regions. |
| Quantity | 7960 downloads |
| Recall Reason | A710 Intellis Clinician Application has a software issue that can result in the inability to program the Intellis implantable neurostimulation device. |
| Device Classification | 20210120 |
| Device Code Info | Software version 1.3.80 |
| Center Classification Date | 20210114 |
| Recall Initiation Date | 20201112 |
| Recalling Firm | Medtronic Neuromodulation |
| Initial Notification | Letter |
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