BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1062763 · Received June 18, 2008

    Report

    Report Number
    1824206-2008-02680
    Event Type
    Malfunction
    Date Received
    June 18, 2008
    Date of Event
    May 23, 2008
    Report Date
    May 23, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    FAC ALLEGED BED WAS ARCING. THE POWER RESISTOR HAS BEEN ORDERED AND ARRIVED AT THIS FACULTY FOR THIS BED. HOWEVER, THE ACCOUNT CANNOT PROVIDE ACCESS TO BEDS WITH PTS ON THEM. TSR WILL INSTALL THIS KIT ON THIS BED WHEN THE BED BECOMES AVAILABLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE AC POWERED HOSPITAL BED FNL HILL-ROM RITTER P3200 NA

    Patients

    Seq Age Sex Outcome Treatment
    1