ESPRIT VENTILATOR Adverse Event — Malfunction (MDR 2031642-2020-01552)
ESPRIT VENTILATOR Adverse Event — Malfunction (MDR 2031642-2020-01552) 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 | 2031642-2020-01552 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | USER FACILITY |
| Narrative | G4:23NOV2020; B4:30NOV2020. THE BLOWER MOTOR ASSEMBLY, MOOG MOTOR WAS RECEIVED FOR EVALUATION. FAILURE ANALYSIS ON THE RETURNED MOOG BLOWER SHOWS THAT THIS CUSTOMER COMPLAINT WAS CAUSED BY SHORTED WINDINGS AT COIL A AND COIL B. SUBMISSION OF A REPORT DOES NOT CONSTITUTE AN ADMISSION THAT MEDICAL PERSONNEL, USER FACILITY, IMPORTER, DISTRIBUTOR, MANUFACTURER, OR PRODUCT CAUSED OR CONTRIBUTED TO THE |
| Source | openFDA MAUDE (device adverse events) |
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