UNI-VENT, MODEL 731 Adverse Event — Malfunction (MDR 1220908-2020-01095)
UNI-VENT, MODEL 731 Adverse Event — Malfunction (MDR 1220908-2020-01095) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNI-VENT, MODEL 731; Generic name: VENTILATOR; Manufacturer: ZOLL MEDICAL CORPORATION.
| Device | UNI-VENT, MODEL 731 |
|---|---|
| Generic name | VENTILATOR |
| Manufacturer | ZOLL MEDICAL CORPORATION |
| Report number | 1220908-2020-01095 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | ZOLL MEDICAL CORPORATION HAS RECEIVED THE PRODUCT AND WILL BE PROVIDING A SUPPLEMENTAL REPORT WHEN OUR INVESTIGATION IS COMPLETED. |
| Source | openFDA MAUDE (device adverse events) |
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