• 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 SUNBEAM; HEATING PAD

  • 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 SUNBEAM; HEATING PAD Back to Search Results
Model Number 832
Device Problem Fire (1245)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  malfunction  
Event Description
Consumer alleges that while using a heating pad for his back it caught on fire and damaged his bedding.No injuries were reported with this incident.
 
Manufacturer Narrative
The product has been requested from the consumer to determine if the incident arose from abuse/misuse of the pad (i.E.Bunching/folding/crushing).A prepaid label was sent to the consumer for return of the product.The consumer has not returned the product.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
SUNBEAM
Type of Device
HEATING PAD
Manufacturer (Section D)
SUNBEAM PRODUCTS, INC, DBA JARDEN CONSUMER SOLUTIONS
2381 executive center dr
boca raton FL 0000
Manufacturer (Section G)
SKY EAGLE HOLDINGS CORP, EAGLE ELECTRIC SHENSHEN
no. 128, chung hwa rd
sec. 2, tucheg
taipei hsien 236
TW   236
Manufacturer Contact
tracie jones
po box 2391
wichita, KS 67201
3162197325
MDR Report Key3716494
MDR Text Key4335571
Report Number3007790958-2014-00054
Device Sequence Number1
Product Code IRT
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 Not Applicable
Type of Report Initial
Report Date 03/25/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received03/25/2014
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Other
Device Model Number832
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? 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
-
-