LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER Adverse Event — Malfunction (MDR 3015876-2008-00073)
LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER Adverse Event — Malfunction (MDR 3015876-2008-00073) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER; Manufacturer: PHYSIO-CONTROL, INC.; Report number: 3015876-2008-00073.
| Device | LIFEPAK 10 DEFIBRILLATOR/MONITOR/PACEMAKER |
|---|---|
| Manufacturer | PHYSIO-CONTROL, INC. |
| Report number | 3015876-2008-00073 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-19 |
| Report source | Health Professional, User facility, Company representation |
| Narrative | THE RPTR CONTACTED PHYSIO-CONTROL TO INQUIRE ABOUT REPLACING THE DEVICE'S DEFIBRILLATION CABLE. ACCORDING TO THE RPTR, THE CABLE HAS THREE "HOLES" AND THE DEFIBRILLATOR HAD ARCED TO A PT'S SHEET'S DURING A CODE. THE RPTR STATED THAT THE PT WAS "OK" AND INDICATED THAT THERE WERE NO ADVERSE AFFECTS TO THE PT AS A RESULT OF THE DEVICE USE. |
| Source | openFDA MAUDE (device adverse events) |
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