BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1062747 · Received June 18, 2008

    Report

    Report Number
    1824206-2008-02647
    Event Type
    Malfunction
    Date Received
    June 18, 2008
    Date of Event
    May 28, 2008
    Report Date
    May 28, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Removal / Correction Number
    Z-0240-2008
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CUSTOMER ALLEGED THAT THE RIGHT RAIL IS NOT STAYING IN THE UP POSITION. CUSTOMER STATED THAT THE PATIENT WAS NOT INJURED DUE TO THE RIGHT SIDERAIL NOT LATCHING. TECHNICIAN FOUND THAT MODIFICATION 380 HAD NOT BEEN PERFORMED ON THIS BED. HE PERFORMED MODIFICATION 380 AND THE SIDERAILS FUNCTIONED PROPERLY.

    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 NA