PD1200 DEFIBRILLATOR/PACEMAKER Adverse Event — Malfunction (MDR 1220908-1997-00103)
PD1200 DEFIBRILLATOR/PACEMAKER Adverse Event — Malfunction (MDR 1220908-1997-00103) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: PD1200 DEFIBRILLATOR/PACEMAKER; Generic name: DEFIBRILLATOR; Manufacturer: ZOLL MEDICAL CORP..
| Device | PD1200 DEFIBRILLATOR/PACEMAKER |
|---|---|
| Generic name | DEFIBRILLATOR |
| Manufacturer | ZOLL MEDICAL CORP. |
| Report number | 1220908-1997-00103 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 1997-06-20 |
| Report source | Health Professional, User facility |
| Narrative | THE STAFF WAS ATTEMPTING AN ELECTIVE CARDIOVERSION OF A PT (AGE AND GENDER UNKNOWN). THE DEVICE WAS IN BATTERY MODE, AND THE STAFF ATTEMPTED TO CHARGE THE DEVICE TO 200 JOULES, WHEN THE DEVICE SHUT DOWN. THE STAFF WAS ABLE TO OBTAIN ANOTHER DEVICE WHEN THE ALLEGED MALFUNCTION OCCURRED. THERE WAS NO ADVERSE EFFECT ON THE PT. |
| Source | openFDA MAUDE (device adverse events) |
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