X SERIES Adverse Event — Malfunction (MDR 1220908-2020-01212)
X SERIES Adverse Event — Malfunction (MDR 1220908-2020-01212) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: X SERIES; Generic name: DEFIBRILLATOR/PACEMAKER; Manufacturer: ZOLL MEDICAL CORPORATION.
| Device | X SERIES |
|---|---|
| Generic name | DEFIBRILLATOR/PACEMAKER |
| Manufacturer | ZOLL MEDICAL CORPORATION |
| Report number | 1220908-2020-01212 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN |
| Narrative | ZOLL MEDICAL CORPORATION HAS NOT RECEIVED THE DEVICE FOR EVALUATION AND THIS COMPLAINT IS STILL UNDER INVESTIGATION. |
| Source | openFDA MAUDE (device adverse events) |
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