CAPSURE SP NOVUS LEAD Adverse Event — Injury (MDR 2649622-2020-08297)
CAPSURE SP NOVUS LEAD Adverse Event — Injury (MDR 2649622-2020-08297) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CAPSURE SP NOVUS LEAD; Generic name: ELECTRODE, PACEMAKER, PERMANENT; Manufacturer: MPRI.
| Device | CAPSURE SP NOVUS LEAD |
|---|---|
| Generic name | ELECTRODE, PACEMAKER, PERMANENT |
| Manufacturer | MPRI |
| Report number | 2649622-2020-08297 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | CONCOMITANT MEDICAL PRODUCTS: A2DR01 IPG IMPLANT DATE (B)(6) 2016. 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 →