INTERSTIM II Adverse Event — Malfunction (MDR 3004209178-2020-07717)
INTERSTIM II Adverse Event — Malfunction (MDR 3004209178-2020-07717) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: INTERSTIM II; Generic name: STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE; Manufacturer: MEDTRONIC PUERTO RICO OPERATIONS CO..
| Device | INTERSTIM II |
|---|---|
| Generic name | STIMULATOR, ELECTRICAL, IMPLANTABLE, FOR INCONTINENCE |
| Manufacturer | MEDTRONIC PUERTO RICO OPERATIONS CO. |
| Report number | 3004209178-2020-07717 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | CONSUMER |
| Narrative | PRODUCT ID: A520, SERIAL# UNKNOWN, PRODUCT TYPE: SOFTWARE. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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