BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE BARIATRIC

    MDR report key: 1888041 · Received October 27, 2010

    Report

    Report Number
    1824206-2010-10711
    Event Type
    Malfunction
    Date Received
    October 27, 2010
    Date of Event
    October 2, 2010
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE BED HAD NOT POWER, THE SERVICE LIGHT WAS ON, AND THE GCI WAS OFF NOT ALLOWING THE TECHNICIAN TO CHECK THE CODES ON THE GCI. THE TECHNICIAN REPLACED A DAMAGED CABLE ASSEMBLY TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE BED IS NOT FUNCTIONING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE BARIATRIC AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1840

    Patients

    Seq Age Sex Outcome Treatment
    1