BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 1952693 · Received January 4, 2011

    Report

    Report Number
    1824206-2011-00031
    Event Type
    Malfunction
    Date Received
    January 4, 2011
    Date of Event
    December 7, 2010
    Report Date
    December 7, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SC, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ACCOUNT REPLACED THE LEFT HEAD COILED CABLE TO RESOLVE THE ALLEGED PROBLEM WITH THE CABLE HAVING BARE METAL WIRES EXPOSED AND THE SERVICE REQUIRED FLASHING AN ERROR CODE.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THEY ARE GETTING SERVICE REQUIRED CODE. ACCOUNT FOUND THE LEFT COILED CABLE HAD CUT EXPOSED WIRES. NO INJURIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSACARE BED A/C POWERED ADJUSTABLE HOSPITAL BED FNL HILL-ROM INC. 3200

    Patients

    Seq Age Sex Outcome Treatment
    1