• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SUNBEAM PRODUCTS INC, DBA JARDEN CONSUMER SOLUTIONS HOLMES; HUMIDIFIER

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

SUNBEAM PRODUCTS INC, DBA JARDEN CONSUMER SOLUTIONS HOLMES; HUMIDIFIER Back to Search Results
Model Number HM5305
Device Problems Break (1069); Fire (1245)
Patient Problem No Consequences Or Impact To Patient (2199)
Event Type  malfunction  
Event Description
Consumer alleges her humidifier caught fire and damaged a table and drywall.There was not a report of injury with this incident.
 
Manufacturer Narrative
A prepaid label has been sent to the consumer for return of the product.Consumer has not returned the product.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
HOLMES
Type of Device
HUMIDIFIER
Manufacturer (Section D)
SUNBEAM PRODUCTS INC, DBA JARDEN CONSUMER SOLUTIONS
2381 executive center dr
boca raton FL
Manufacturer (Section G)
DONGGUAN HUIXAN ELECTRICAL PRODUCTS
no. 9112, hung yeh 8th rd
tangxia town, dongguan
CH  
Manufacturer Contact
tracie jones
p.o. box 2931
wichita, KS 67201
3162197325
MDR Report Key4511913
MDR Text Key17577783
Report Number3003862163-2015-00022
Device Sequence Number1
Product Code KFZ
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Consumer
Reporter Occupation Other
Type of Report Initial
Report Date 02/05/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received02/05/2015
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Model NumberHM5305
Was Device Available for Evaluation? No
Was Device Evaluated by Manufacturer? No
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Unknown
Patient Sequence Number1
-
-