HEARTSTART MRX - EMS DEFIBRILLATOR Adverse Event — Malfunction (MDR 1218950-2008-00125)
HEARTSTART MRX - EMS DEFIBRILLATOR Adverse Event — Malfunction (MDR 1218950-2008-00125) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: HEARTSTART MRX - EMS DEFIBRILLATOR; Generic name: DEFIBRILLATOR; Manufacturer: PHILIPS MEDICAL SYSTEMS.
| Device | HEARTSTART MRX - EMS DEFIBRILLATOR |
|---|---|
| Generic name | DEFIBRILLATOR |
| Manufacturer | PHILIPS MEDICAL SYSTEMS |
| Report number | 1218950-2008-00125 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2008-02-21 |
| Report source | Health Professional, User facility, Company representation |
| Narrative | THE CUSTOMER REPORTED THAT THE DISPLAY WAS NOT READABLE. |
| Source | openFDA MAUDE (device adverse events) |
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