SPRINT Adverse Event — Malfunction (MDR 2649622-2020-08316)
SPRINT Adverse Event — Malfunction (MDR 2649622-2020-08316) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SPRINT; Generic name: DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER; Manufacturer: MPRI.
| Device | SPRINT |
|---|---|
| Generic name | DEFIBRILLATOR, AUTOMATIC IMPLANTABLE CARDIOVERTER |
| Manufacturer | MPRI |
| Report number | 2649622-2020-08316 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | CONCOMITANT MEDICAL PRODUCTS: 419388 LEAD, IMPLANTED (B)(6) 2004. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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