BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1082381 · Received July 25, 2008

    Report

    Report Number
    1824206-2008-02899
    Event Type
    Malfunction
    Date Received
    July 25, 2008
    Date of Event
    May 28, 2008
    Report Date
    May 28, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IN 2008 - REP ALLEGED THAT THE RH INTERMEDIATE SIDERAIL WILL NOT LATCH. NO INJURIES REPORTED AT THIS TIME. THE FOLLOWING MONTH - SUM - REP STATED THAT THE LATCH AND LATCH PIN WERE SLIGHTLY WORN FROM USE. REP STATED THAT HE REPLACED THE SIDERAIL LATCH AND LATCH PIN TO REPAIR THE SIDERAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TOTALCARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER 1900 P1900D003430

    Patients

    Seq Age Sex Outcome Treatment
    1