BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1191300 · Received September 26, 2008

    Report

    Report Number
    1824206-2008-03606
    Event Type
    Malfunction
    Date Received
    September 26, 2008
    Date of Event
    September 2, 2008
    Report Date
    September 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

    A HILL-ROM TECHNICAL SERVICE REPRESENTATIVE ALLEGED THAT THE SCALE WAS READING HEAVY. THE TSR STATED THAT THERE WAS NOT A PT IN THE BED AND THE BED WAS IN THE MAINTENANCE SHOP. HE STATED THAT HE CALIBRATED THE SCALE TO RESOLVE THE PROBLEM.

    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