ACTIVA Adverse Event — Malfunction (MDR 3004209178-2020-07787)
ACTIVA Adverse Event — Malfunction (MDR 3004209178-2020-07787) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ACTIVA; Generic name: STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO..
| Device | ACTIVA |
|---|---|
| Generic name | STIMULATOR, ELECTRICAL, IMPLANTED, FOR PARKINSONIAN TREMOR |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2020-07787 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, CONSUM |
| Narrative | IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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