INTELLIS Adverse Event — Malfunction (MDR 3004209178-2020-07766)
INTELLIS Adverse Event — Malfunction (MDR 3004209178-2020-07766) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTELLIS; Generic name: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO..
| Device | INTELLIS |
|---|---|
| Generic name | STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2020-07766 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | CONSUMER |
| Narrative | ADDITIONAL INFORMATION WAS RECEIVED. IT WAS REPORTED THE PATIENT WAS HAVING PAIN AND THEIR FEET WERE NUMB. THE CALLER STATED THEY THINK IT NEEDED A BATTERY. NO FURTHER COMPLICATIONS WERE REPORTED OR ANTICIPATED. |
| Source | openFDA MAUDE (device adverse events) |
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