FDA Adverse Event Injury Summary report: N

SUNBEAM

MDR report key: 6015495 · Received October 10, 2016

Report

Report Number
3003862163-2016-00166
Event Type
Injury
Date Received
October 10, 2016
Date of Event
September 19, 2016
Report Date
October 10, 2016
Manufacturer
SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTI
Product Code
KFZ
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MT, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

CONSUMER ALLEGES THAT HER HUMIDIFIER MELTED AND EMITTED SMOKE. SHE ALSO CLAIMS THAT HER FOOT WAS BURNED WHEN SHE STEPPED ON SOME MELTED MATERIAL AND THAT HER DAUGHTER SUFFERED FROM SMOKE INHALATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
665143 SUNBEAM HUMIDIFIER KFZ SUNBEAM PRODUCTS, INC., DBA JARDEN CONSUMER SOLUTI SWM6000-NWM2

Patients

Seq Age Sex Outcome Treatment
1 Other