BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 3061375 · Received March 26, 2013

    Report

    Report Number
    1824206-2013-01687
    Event Type
    Malfunction
    Date Received
    March 26, 2013
    Date of Event
    January 23, 2013
    Report Date
    February 27, 2013
    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

    NO FURTHER INFORMATION IS AVAILABLE ON THE REPAIR OF THE BED AT THIS TIME.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD OF THE BED HAS NOT FUNCTIONS AND THE HEAD OF THE BED IS RAISED. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    124611 RESIDENT BED AC POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 870

    Patients

    Seq Age Sex Outcome Treatment
    1