BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    RESIDENT BED

    MDR report key: 2212863 · Received July 12, 2011

    Report

    Report Number
    1824206-2011-03691
    Event Type
    Malfunction
    Date Received
    July 12, 2011
    Date of Event
    June 28, 2011
    Report Date
    June 28, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNTS MAINTENANCE ISOLATED THE ISSUE TO THE LOCKOUT BOX. HE REPLACED THE LOCKOUT BOX TO REPAIR THE BED.

    Description of Event or Problem · 1

    THE ACCOUNTS MAINTENANCE STATED THE HEAD AND KNEE WILL NOT LOWER AND BOTH ARE IN THE RAISED POSITION. HE HAS REPLACED THE HAND PENDANT AND CONTROL BOX AND STILL HAS SAME ISSUE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1