BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SKYTRON 6500HD

    MDR report key: 623696 · Received July 18, 2005

    Report

    Report Number
    623696
    Event Type
    Malfunction
    Date Received
    July 18, 2005
    Date of Event
    July 7, 2005
    Report Date
    July 8, 2005
    Manufacturer
    SKYTRON, DIV. OF KMW GRP.
    Product Code
    FQO
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    IL, US

    Narratives

    Description of Event or Problem · 1

    THE TAPERED PIN LOCKING THE ENTIRE OPERATING TABLE TO THE COLUMN TRENDELENBURG GEAR SLIPPED HALF-WAY OUT, ALLOWING THE ENTIRE TABLETOP TO WOBBLE VERTICALLY ABOUT 6".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SKYTRON 6500HD SURGICAL TABLE FQO SKYTRON, DIV. OF KMW GRP. 6500HD N/A

    Patients

    Seq Age Sex Outcome Treatment
    1 *