BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    VERSACARE BED

    MDR report key: 1961342 · Received December 20, 2010

    Report

    Report Number
    1824206-2010-11756
    Event Type
    Malfunction
    Date Received
    December 20, 2010
    Date of Event
    October 27, 2010
    Report Date
    November 30, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN ORDERED A COILED CABLE. NO FURTHER INFO ON THE REPAIR IS AVAILABLE AT THIS TIME.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT THE SIDERAIL HAS NO POWER. TECHNICIAN FOUND THAT THE INSULATION IS CUT, THE CABLE HAS BEEN PINCHED AND THERE ARE BARE METAL WIRES SHOWING. NO INJURIES WERE REPORTED.

    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