M SERIES Adverse Event — Death (MDR 1220908-2007-02741)
M SERIES Adverse Event — Death (MDR 1220908-2007-02741) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: M SERIES; Generic name: DEFIBRILLATOR/PACEMAKER; Manufacturer: ZOLL MEDICAL CORPORATION.
| Device | M SERIES |
|---|---|
| Generic name | DEFIBRILLATOR/PACEMAKER |
| Manufacturer | ZOLL MEDICAL CORPORATION |
| Report number | 1220908-2007-02741 |
| Event type | Death |
| Product problem | N |
| Date received | 2007-12-19 |
| Report source | Health Professional, User facility |
| Narrative | TWO DEVICES WERE USED DURING THE EVENT. THE OTHER DEVICE IS BEING REPORTED UNDER MEDWATCH #1220908-2007-02741. PLEASE REFER TO A COPY OF THE ATTACHED USER MEDWATCH REPORT. ZOLL MEDICAL CORPORATION HAS NOT RECEIVED THE PRODUCT AND THIS COMPLAINT IS STILL UNDER INVESTIGATION. |
| Source | openFDA MAUDE (device adverse events) |
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