BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HILL-ROM 1000 BED

    MDR report key: 1946046 · Received December 21, 2010

    Report

    Report Number
    3006697241-2010-00058
    Event Type
    Malfunction
    Date Received
    December 21, 2010
    Date of Event
    November 22, 2010
    Report Date
    November 22, 2010
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH FOUND WHEN THE BED IS ON THE LIFT, THE BRAKE AND STEER SETS PERFECTLY, BUT ONCE THE BED IS LOWERED TO THE GROUND, THE BRAKES WILL NOT HOLD. REPAIRS HAVE NOT BEEN COMPLETED.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE BED WOULD NOT LOCK IN THE BRAKE MODE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HILL-ROM 1000 BED AC-POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM DE MEXICO S DE RL DE CV 1160

    Patients

    Seq Age Sex Outcome Treatment
    1