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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SUNBEAM PRODUCTS, INC. DBA JARDEN CONSUMER SOLUTIONS SUNBEAM; HEATING PAD

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SUNBEAM PRODUCTS, INC. DBA JARDEN CONSUMER SOLUTIONS SUNBEAM; HEATING PAD Back to Search Results
Device Problem Failure to Shut Off (2939)
Patient Problem Full thickness (Third Degree) Burn (2696)
Event Type  Injury  
Event Description
Consumer claims she was using a heating pad and her neck was burned after the auto-off did not work.She is alleging 3rd degree burns and attempted self-treatment, but eventually sought medical care.
 
Manufacturer Narrative
There is an instruction that states, "burns can occur regardless of control setting.Check skin under pad frequently" and consumer failed to perform that instruction.The pad has been requested from the consumer to determine if the incident arose from abuse/misuse of the pad (i.E.Bunching/folding/crushing).
 
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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
Manufacturer (Section G)
SKYEAGLE HOLDINGS CORP
eagle electric shenshen
no. 128, ching hwa rd., sec 2, tucheg
taipei hsien 236
CH   236
Manufacturer Contact
tracie jones
po box 2391
wichita, KS 67201
3162197325
MDR Report Key3843823
MDR Text Key17290809
Report Number3007790958-2014-00093
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 05/23/2014
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received05/27/2014
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Other
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
Patient Outcome(s) Other;
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