ESPRIT VENTILATOR Adverse Event — Malfunction (MDR 2031642-2020-01563)
ESPRIT VENTILATOR Adverse Event — Malfunction (MDR 2031642-2020-01563) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ESPRIT VENTILATOR; Generic name: VENTILATOR; Manufacturer: RESPIRONICS CALIFORNIA, INC.
| Device | ESPRIT VENTILATOR |
|---|---|
| Generic name | VENTILATOR |
| Manufacturer | RESPIRONICS CALIFORNIA, INC |
| Report number | 2031642-2020-01563 |
| 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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