BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1052198 · Received May 21, 2008

    Report

    Report Number
    1824206-2008-02572
    Event Type
    Malfunction
    Date Received
    May 21, 2008
    Date of Event
    May 2, 2008
    Report Date
    May 2, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    TSR FOUND THAT THE RIGHT HEAD SIDERAIL LATCH PINS (PART NUMBERS 140866 AND 140867) HAD STICKY SUBSTANCE ON THE LATCH PINS. HE CLEANED AND LUBRICATED THE LATCH PINS AND THE RIGHT HEAD SIDERAIL 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