BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 1082080 · Received July 25, 2008

    Report

    Report Number
    1824206-2008-02909
    Event Type
    Malfunction
    Date Received
    July 25, 2008
    Date of Event
    June 24, 2008
    Report Date
    June 24, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE HILL-ROM FIELD TECHNICIAN FOUND THAT THE BRAKES WOULD NOT HOLD ON THIS BED. HE FOUND THAT THE CASTERS WERE WORN DUE TO THE AGE OF THE BED. HE REPLACED THE CASTERS TO CORRECT THE ISSUE. NO INCIDENTS OR INJURIES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CENTRA BED AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 850 NA

    Patients

    Seq Age Sex Outcome Treatment
    1