HEARTSTART XL+ DEFIBRILLATOR/MONITOR Adverse Event — Malfunction (MDR 1218950-2020-02528)
HEARTSTART XL+ DEFIBRILLATOR/MONITOR Adverse Event — Malfunction (MDR 1218950-2020-02528) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: HEARTSTART XL+ DEFIBRILLATOR/MONITOR; Generic name: ALS DEFIBRILLATOR MONITOR; Manufacturer: PHILIPS MEDICAL SYSTEMS.
| Device | HEARTSTART XL+ DEFIBRILLATOR/MONITOR |
|---|---|
| Generic name | ALS DEFIBRILLATOR MONITOR |
| Manufacturer | PHILIPS MEDICAL SYSTEMS |
| Report number | 1218950-2020-02528 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN, USER FACILITY |
| Narrative | A FOLLOW-UP REPORT WILL BE SUBMITTED ONCE THE INVESTIGATION IS COMPLETED. |
| Source | openFDA MAUDE (device adverse events) |
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