CAPSURE SP Adverse Event — Injury (MDR 2182208-2020-00820)
CAPSURE SP Adverse Event — Injury (MDR 2182208-2020-00820) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CAPSURE SP; Generic name: ELECTRODE, PACEMAKER, PERMANENT; Manufacturer: MEDTRONIC, INC..
| Device | CAPSURE SP |
|---|---|
| Generic name | ELECTRODE, PACEMAKER, PERMANENT |
| Manufacturer | MEDTRONIC, INC. |
| Report number | 2182208-2020-00820 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →