BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 2003194 · Received February 22, 2011

    Report

    Report Number
    1824206-2011-01009
    Event Type
    Malfunction
    Date Received
    February 22, 2011
    Date of Event
    January 28, 2011
    Report Date
    January 28, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN FOUND THE BRAKE CASTER LOOKED OLD AND WORN. WHEN HE APPLIED THE BRAKE AND ROCKED THE BED, THE BRAKE PEDAL WENT INTO NEUTRAL. HE INSPECTED THE BRAKE MECHANISM AND FOUND THE CABLE WAS KINKED AND FRAYED. HE REPLACED THE BRAKE MECHANISM AND ATTEMPTED TO ADJUST THE ALLEN SCREW ON THE BRAKE CASTER BUT IT WOULD NOT LOCK. HE REPLACED THE BRAKE CASTER TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE BRAKES WILL NOT STAY SET.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1