BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1010529 · Received February 6, 2008

    Report

    Report Number
    1010529
    Event Type
    Malfunction
    Date Received
    February 6, 2008
    Date of Event
    February 4, 2008
    Report Date
    February 6, 2008
    Manufacturer
    SKYTRON
    Product Code
    FQO
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US

    Narratives

    Description of Event or Problem · 1

    THE PATIENT WAS TILTED ON THE OR BED (TABLE) TO THE LEFT DURING SURGERY. WHEN THE PHYSICIAN ASKED TO TILT THE PATIENT BACK TO THE MIDLINE POSITION, THE OR BED (TABLE) WOULD NOT MOVE. THE MOTOR WAS MAKING NOISE BUT THE BED (TABLE) WAS NOT MOVING. TWO PHYSICIANS HAD TO PULL UP ON THE FRAME OF THE BED (TABLE) TO GET THE BED (TABLE) TO MOVE TO THE CENTER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * TABLE, SURGICAL FQO SKYTRON * *

    Patients

    Seq Age Sex Outcome Treatment
    1 *