V60 VENTILATOR Adverse Event — Malfunction (MDR 2031642-2020-01588)
V60 VENTILATOR Adverse Event — Malfunction (MDR 2031642-2020-01588) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: V60 VENTILATOR; Generic name: VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY; Manufacturer: RESPIRONICS CALIFORNIA, INC.
| Device | V60 VENTILATOR |
|---|---|
| Generic name | VENTILATOR, CONTINUOUS, MINIMAL VENTILATORY SUPPORT,FACILITY |
| Manufacturer | RESPIRONICS CALIFORNIA, INC |
| Report number | 2031642-2020-01588 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN, HEALTH PROFESSIONAL |
| Narrative | G4: 23APR2020. B4: 22JUN2020. THIS EVENT WAS CLARIFIED AS HAVING OCCURRED DURING PATIENT USE - THERE WAS NO ALLEGATION OF HARM ASSOCIATED WITH THIS EVENT. SUBMISSION OF A REPORT DOES NOT CONSTITUTE AN ADMISSION THAT MEDICAL PERSONNEL, USER FACILITY, IMPORTER, DISTRIBUTOR, MANUFACTURER, OR PRODUCT CAUSED OR CONTRIBUTED TO THE EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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