BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TOTALCARE

    MDR report key: 1250647 · Received November 14, 2008

    Report

    Report Number
    1824206-2008-04196
    Event Type
    Malfunction
    Date Received
    November 14, 2008
    Date of Event
    October 17, 2008
    Report Date
    October 17, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OH, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    THE HILL-ROM TECH REMOVED, CLEANED AND REINSTALLED THE HEAD HI/LOW VALVE TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATES THE HEAD HI/LOW FUNCTION OF THE BED IS DRIFTING DOWN. A PT IS IN TRACTION ON THE BED, BUT WAS NOT INJURED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK