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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MOBILE COMPUTER CART; MEDICAL COMPUTERS AND SOFTWARE

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MOBILE COMPUTER CART; MEDICAL COMPUTERS AND SOFTWARE Back to Search Results
Device Problem Smoking (1585)
Patient Problem No Known Impact Or Consequence To Patient (2692)
Event Date 07/21/2017
Event Type  malfunction  
Event Description
Battery/inverter unit for mobile medical computer cart plugged in to wall outlet began to smoke heavily during episode of pt care.Therapy duration: 1 year.Diagnosis or reason for use: electronic documentation.Event abated after use stopped or dose reduced: yes.
 
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Brand Name
MOBILE COMPUTER CART
Type of Device
MEDICAL COMPUTERS AND SOFTWARE
MDR Report Key6785200
MDR Text Key82565713
Report NumberMW5071489
Device Sequence Number1
Product Code LNX
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Other Health Care Professional
Type of Report Initial
Report Date 08/08/2017
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received08/08/2017
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator No Information
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? Yes
Was Device Evaluated by Manufacturer? No Information
Type of Device Usage N
Patient Sequence Number1
Patient Outcome(s) Other;
Patient Age63 YR
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