M SERIES Adverse Event — Malfunction (MDR 1220908-2008-00282)
M SERIES Adverse Event — Malfunction (MDR 1220908-2008-00282) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: M SERIES; Generic name: DEFIBRILLATOR/PACEMAKER; Manufacturer: ZOLL MEDICAL CORP..
| Device | M SERIES |
|---|---|
| Generic name | DEFIBRILLATOR/PACEMAKER |
| Manufacturer | ZOLL MEDICAL CORP. |
| Report number | 1220908-2008-00282 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-15 |
| Report source | Health Professional, User facility |
| Narrative | ZOLL MEDICAL CORP HAS NOT REC'D THE DEVICE FOR EVAL AND THIS COMPLAINT IS STILL UNDER INVESTIGATION. |
| Source | openFDA MAUDE (device adverse events) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →