AIRVO 2 HUMIDIFIER Adverse Event — Malfunction (MDR 9611451-2020-00407)
AIRVO 2 HUMIDIFIER Adverse Event — Malfunction (MDR 9611451-2020-00407) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: AIRVO 2 HUMIDIFIER; Generic name: AIRVO 2 HUMIDIFIER; Report number: 9611451-2020-00407.
| Device | AIRVO 2 HUMIDIFIER |
|---|---|
| Generic name | AIRVO 2 HUMIDIFIER |
| Report number | 9611451-2020-00407 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | HEALTH PROFESSIONAL, USER FACI |
| Narrative | (B)(4). METHOD: THE COMPLAINT MYAIRVO HUMIDIFIER WAS RECEIVED AT FISHER & PAYKEL HEALTHCARE (F&P) AND WAS VISUALLY INSPECTED AND ELECTRICALLY TESTED. RESULTS: DURING TESTING IT WAS FOUND THAT THE AUDIBLE ALARM DID NOT FUNCTION AND ELECTRICAL RESISTANCE TESTING HAS SHOWN THE SPEAKER'S RESISTANCE TO BE OPEN CIRCUIT. CONCLUSION: AS PART OF OUR ONGOING PRODUCT IMPROVEMENT INITIATIVES, WE HAVE IMPLEMEN |
| Source | openFDA MAUDE (device adverse events) |
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