BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE

    MDR report key: 1191365 · Received September 26, 2008

    Report

    Report Number
    1824206-2008-03609
    Event Type
    Malfunction
    Date Received
    September 26, 2008
    Date of Event
    September 18, 2008
    Report Date
    September 18, 2008
    Manufacturer
    HILL-ROM RITTER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CUSTOMER ALLEGED THAT THE POWER CORD IS CUT AND THE BARE METAL GROUND WIRE IS EXPOSED. THEY STATED THAT THERE WERE NO INJURIES AND A PATIENT WAS NOT IN THE BED. CUSTOMER STATED THEY REMOVED ABOUT A FOOT SECTION OF THE DAMAGED POWER CORD (TOWARD THE BOARD SIDE OF THE CORD) AND THEN PROPERLY RECONNECTED THE CORD TO RESOLVE THIS ISSUE. BED WAS RETURNED TO SERVICE.

    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