MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-02-19 for HONEYWELL HWM-340B manufactured by Honeywell International Inc./kaz Usa, Inc., A Helen Of Troy Company.
[136538466]
Our honeywell humidifier model hwm-340b caught on fire. The unit had been running for a period of approximately 4 hours. We did not refill the unit with water and the unit went dry. The unit overheated and burst into flames. Fortunately we were able to douse the fire and sustained no damage to our house. Incident location: home/apartment/condominium - (b)(6), united states. This is my home address. Purchase date: (b)(6) 2018. Explanation: i notified honeywell and i have the damaged humidifier. (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5084158 |
| MDR Report Key | 8351180 |
| Date Received | 2019-02-19 |
| Date of Event | 2019-01-27 |
| Date Added to Maude | 2019-02-19 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Reporter Occupation | PATIENT |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | HONEYWELL |
| Generic Name | HUMIDIFIER, NON-DIRECT PATIENT INTERFACE (HOME-USE) |
| Product Code | KFZ |
| Date Received | 2019-02-19 |
| Model Number | HWM-340B |
| Device Availability | Y |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | HONEYWELL INTERNATIONAL INC./KAZ USA, INC., A HELEN OF TROY COMPANY |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-02-19 |