BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CENTRA BED

    MDR report key: 1051195 · Received May 22, 2008

    Report

    Report Number
    1824206-2008-02573
    Event Type
    Malfunction
    Date Received
    May 22, 2008
    Date of Event
    April 25, 2008
    Report Date
    April 28, 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

    HOSPITAL BIOMED CALLED AND ALLEGED THE BED LOWERED SUDDENLY WITH A PATIENT ON THE BED. REPORTER STATED THAT SHE WAS NOT AWARE OF ANY PATIENT INJURIES. THE HILL-ROM TECHNICIAN EXAMINED THE BED AND FOUND THAT A BOLT THAT SECURES THE TIE ROD TO THE PIVOT PLATE HAD BROKEN WHICH CAUSED THE BED TO LOWER SUDDENLY. HE REPAIRED THE BED BY REPLACING THE BOLT AND THE PIVOT PLATE. THE BED FUNCTIONED AS DESIGNED AFTER THE REPAIR.

    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 UNK