FDA Adverse Event Malfunction Summary report: N

BIONAIRE

MDR report key: 3834395 · Received May 12, 2014

Report

Report Number
3003862163-2014-00086
Event Type
Malfunction
Date Received
May 12, 2014
Date of Event
March 1, 2014
Report Date
May 12, 2014
Manufacturer
SUNBEAM PRODUCTS, INC. DBA JARDEN CONSUMER SOLUTIONS
Product Code
KFZ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IN, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THIS PRODUCT IS IN THE POSSESSION OF THE INSURANCE COMPANY AND HAS NOT BEEN EXAMINED.

Description of Event or Problem · 1

AN INSURANCE COMPANY IS ALLEGING THAT A HUMIDIFIER CAUGHT FIRE AND DAMAGED ITS INSURED'S HOME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
283274 BIONAIRE HUMIDIFIER KFZ SUNBEAM PRODUCTS, INC. DBA JARDEN CONSUMER SOLUTIONS HM5082 UNK

Patients

Seq Age Sex Outcome Treatment
1