BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MAQUET OR TABLE SYSTEM MAGNUS

    MDR report key: 4366313 · Received December 17, 2014

    Report

    Report Number
    3008355164-2014-00371
    Event Type
    Injury
    Date Received
    December 17, 2014
    Date of Event
    November 19, 2014
    Report Date
    November 19, 2014
    Manufacturer
    MAQUET GMBH
    Product Code
    FQO
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    SC, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    DURING SURGERY THE TABLE TOP STOPPED RESPONDING WHEN THE WIRELESS HAND CONTROLLER WAS DEPRESSED. A WIRED HAND CONTROLLER WAS THEN USED AND THE TABLE STARTED TO RESPOND ONLY AFTER SEVERAL ATTEMPTS WERE MADE. THE PATIENT WAS MOVED TO ANOTHER TABLE. THIS CAUSED A DELAY IN THE PROCEDURE. THE PROCEDURE COULD BE FINALIZED SUCCESSFULLY WITH NO INJURY TO THE PATIENT. (B)(4). MFR REF#8010652-2014-00022.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    829249 MAQUET OR TABLE SYSTEM MAGNUS TABLE, OPERATING-ROOM, AC-POWERED FQO MAQUET GMBH 1180.10F0

    Patients

    Seq Age Sex Outcome Treatment
    1 58 YR Required Intervention