BIPAP FOCUS NONINVASIVE VENTILATOR SYSTEM Adverse Event — Malfunction (MDR 2031642-2020-01550)
BIPAP FOCUS NONINVASIVE VENTILATOR SYSTEM Adverse Event — Malfunction (MDR 2031642-2020-01550) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BIPAP FOCUS NONINVASIVE VENTILATOR SYSTEM; Generic name: VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING; Manufacturer: RESPIRONICS CALIFORN
| Device | BIPAP FOCUS NONINVASIVE VENTILATOR SYSTEM |
|---|---|
| Generic name | VENTILATOR, CONTINUOUS, NON-LIFE-SUPPORTING |
| Manufacturer | RESPIRONICS CALIFORNIA, INC |
| Report number | 2031642-2020-01550 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | USER FACILITY |
| Narrative | DATE OF EVENT: (B)(6) 2020. DATE OF REPORT: 27APR2020. |
| Source | openFDA MAUDE (device adverse events) |
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