FDA Adverse Event Malfunction Summary report: N

SUNBEAM

MDR report key: 3881235 · Received February 14, 2014

Report

Report Number
3003862163-2014-00031
Event Type
Malfunction
Date Received
February 14, 2014
Report Date
February 14, 2014
Manufacturer
SUNBEAM PRODUCTS, INC. DBA JARDEN CONSUMER SOLUTIONS
Product Code
KFZ
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

A PREPAID LABEL HAS BEEN SENT TO THE CONSUMER FOR THE RETURN OF THE PRODUCT. CONSUMER HAS NOT RETURNED THE PRODUCT.

Description of Event or Problem · 1

CONSUMER CLAIMS HER HUMIDIFER EMITTED SPARKS AND SMOKE. THERE WAS NO REPORTS OF INJURY OR PROPERTY DAMAGE WITH THIS INCIDENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
97227 SUNBEAM HUMIDIFIER KFZ SUNBEAM PRODUCTS, INC. DBA JARDEN CONSUMER SOLUTIONS SCM3501-115 UNK

Patients

Seq Age Sex Outcome Treatment
1