CAPSUREFIX LEAD Adverse Event — Injury (MDR 2649622-2020-08331)
CAPSUREFIX LEAD Adverse Event — Injury (MDR 2649622-2020-08331) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: CAPSUREFIX LEAD; Generic name: ELECTRODE, PACEMAKER, PERMANENT; Manufacturer: MPRI.
| Device | CAPSUREFIX LEAD |
|---|---|
| Generic name | ELECTRODE, PACEMAKER, PERMANENT |
| Manufacturer | MPRI |
| Report number | 2649622-2020-08331 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, HEALTH |
| Narrative | CONCOMITANT MEDICAL PRODUCTS: SEDR01, IPG, IMPLANT DATE: (B)(6) 2009. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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