VAPOTHERM Adverse Event — Malfunction (MDR 10000413)
VAPOTHERM Adverse Event — Malfunction (MDR 10000413) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: VAPOTHERM; Generic name: HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE); Manufacturer: VAPOTHERM.
| Device | VAPOTHERM |
|---|---|
| Generic name | HUMIDIFIER, RESPIRATORY GAS, (DIRECT PATIENT INTERFACE) |
| Manufacturer | VAPOTHERM |
| Report number | 10000413 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Narrative | VAPOTHERM WAS ON PATIENT, IT STARTED LEAKING WATER. SWITCHED TO ANOTHER VAPOTHERM AND IT WORKED FOR ABOUT 1 MIN AND SHUT OFF. CHANGED TO ANOTHER VAPOTHERM. |
| Source | openFDA MAUDE (device adverse events) |
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