AED PLUS Adverse Event — Malfunction (MDR 1220908-2020-01091)
AED PLUS Adverse Event — Malfunction (MDR 1220908-2020-01091) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AED PLUS; Generic name: DEFIBRILLATOR; Manufacturer: ZOLL MEDICAL CORPORATION.
| Device | AED PLUS |
|---|---|
| Generic name | DEFIBRILLATOR |
| Manufacturer | ZOLL MEDICAL CORPORATION |
| Report number | 1220908-2020-01091 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | FOREIGN |
| Narrative | ZOLL MEDICAL CORPORATION HAS RECEIVED THE PRODUCT AND WILL BE PROVIDING A SUPPLEMENTAL REPORT WHEN OUR INVESTIGATION IS COMPLETED. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →