BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 3004049 · Received February 19, 2013

    Report

    Report Number
    1824206-2013-01011
    Event Type
    Malfunction
    Date Received
    February 19, 2013
    Date of Event
    February 14, 2013
    Report Date
    February 14, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT CALLED BACK TO TROUBLE SHOOT MORE AND STATED THE BED IS NOW FUNCTIONING AS DESIGNED. THE TECHNICIAN TOLD THE ACCOUNT THAT THE RELAY IN THE CONTROL BOX MAY HAVE BEEN STUCK AND IS NOW FUNCTIONING.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGES THE HEAD IS UP AND WILL NOT LOWER. THERE WAS NO REPORTED INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    72490 RESIDENT BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM, INC. 870

    Patients

    Seq Age Sex Outcome Treatment
    1