E SERIES DEFIBRILLATOR Adverse Event — Death (MDR 1220908-2008-00281)
E SERIES DEFIBRILLATOR Adverse Event — Death (MDR 1220908-2008-00281) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: E SERIES DEFIBRILLATOR; Generic name: E SERIES; Manufacturer: ZOLL MEDICAL CORPORATION.
| Device | E SERIES DEFIBRILLATOR |
|---|---|
| Generic name | E SERIES |
| Manufacturer | ZOLL MEDICAL CORPORATION |
| Report number | 1220908-2008-00281 |
| Event type | Death |
| Product problem | N |
| Date received | 2008-02-15 |
| Report source | Health Professional, User facility |
| Narrative | COMPLAINANT ALLEGED THAT WHILE ATTEMPTING TO DEFIBRILLATE A MALE PT, THE DEVICE DISPLAYED "DEFIB FAULT 72" MESSAGE. COMPLAINANT INDICATED THAT THE PT SUBSEQUENTLY EXPIRED. |
| Source | openFDA MAUDE (device adverse events) |
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