V200 VENTILATOR Adverse Event — Malfunction (MDR 2031642-2020-01571)
V200 VENTILATOR Adverse Event — Malfunction (MDR 2031642-2020-01571) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: V200 VENTILATOR; Generic name: VENTILATOR, CONTINUOUS, FACILITY USE; Manufacturer: RESPIRONICS CALIFORNIA, INC.
| Device | V200 VENTILATOR |
|---|---|
| Generic name | VENTILATOR, CONTINUOUS, FACILITY USE |
| Manufacturer | RESPIRONICS CALIFORNIA, INC |
| Report number | 2031642-2020-01571 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | G4: 17MAY2020. B4: 18MAY2020. HE FIELD SERVICE ENGINEER MADE MULTIPLE UNSUCCESSFUL ATTEMPTS TO GATHER RESOLUTION. HOWEVER, THE CUSTOMER WAS NOT AVAILABLE FOR FOLLOW-UP AND NO EMAIL RESPONSE. NO FURTHER INFORMATION AVAILABLE. SUBMISSION OF A REPORT DOES NOT CONSTITUTE AN ADMISSION THAT MEDICAL PERSONNEL, USER FACILITY, IMPORTER, DISTRIBUTOR, MANUFACTURER, OR PRODUCT CAUSED OR CONTRIBUTED TO THE EVE |
| Source | openFDA MAUDE (device adverse events) |
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