• 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. SUNBEAM HEATING PAD FOR PAIN RELIEF KING SIZE ULTRAHEAT, 3 HEAT SETTINGS W/AUTO; PAD, HEATING, POWERED

  • 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. SUNBEAM HEATING PAD FOR PAIN RELIEF KING SIZE ULTRAHEAT, 3 HEAT SETTINGS W/AUTO; PAD, HEATING, POWERED Back to Search Results
Model Number 732-500
Device Problems Thermal Decomposition of Device (1071); Melted (1385)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Type  Injury  
Event Description
I have used the same sunbeam heating pad for the past 7 years in the same location on my couch every night.Tonight, the heating pad was on for approx 15 mins when it become extremely hot.I turned it off and it remained hot.I removed the pad from behind my back and smelled burning plastic.I turned off the heating pad and unplugged it.The plastic pad on the inside was melting and beginning to burn.Retailer: (b)(6).Purchase date: (b)(6) 2012.(b)(4).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
SUNBEAM HEATING PAD FOR PAIN RELIEF KING SIZE ULTRAHEAT, 3 HEAT SETTINGS W/AUTO
Type of Device
PAD, HEATING, POWERED
Manufacturer (Section D)
SUNBEAM PRODUCTS INC.
MDR Report Key8619880
MDR Text Key145482032
Report NumberMW5086699
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 Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 05/06/2019
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator No Information
Device Model Number732-500
Was Device Available for Evaluation? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received05/16/2019
Was Device Evaluated by Manufacturer? No Information
Type of Device Usage N
Patient Sequence Number1
Patient Age36 YR
-
-