BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 2140594 · Received June 16, 2011

    Report

    Report Number
    1824206-2011-03285
    Event Type
    Malfunction
    Date Received
    June 16, 2011
    Date of Event
    May 26, 2011
    Report Date
    May 26, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    THE CUSTOMER STATED THEIR HOUSE LOST POWER LAST NIGHT AND THE BED WOULD NOT OPERATE ON THE BATTERY. THE BATTERY LIGHT WOULD COME ON WHEN THE BED WAS UNPLUGGED AND THEN GO OUT AS HE TRIED TO USE THE MANUAL FUNCTIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 1900

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK