SERVO-S Adverse Event — Malfunction (MDR 8010042-2020-00248)
SERVO-S Adverse Event — Malfunction (MDR 8010042-2020-00248) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SERVO-S; Generic name: VENTILATOR, CONTINUOUS, FACILITY USE; Manufacturer: MAQUET CRITICAL CARE AB.
| Device | SERVO-S |
|---|---|
| Generic name | VENTILATOR, CONTINUOUS, FACILITY USE |
| Manufacturer | MAQUET CRITICAL CARE AB |
| Report number | 8010042-2020-00248 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | IT WAS REPORTED THAT THE VENTILATOR FAILED PRESSURE TRANSDUCER TEST DURING PRE-USE CHECK AND IT DISPLAYED ABNORMAL VENTILATION WAVEFORM DURING TREATMENT. THERE WAS NO PATIENT HARM. MANUFACTURER REF.#: (B)(4). |
| Source | openFDA MAUDE (device adverse events) |
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