BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    4911620

    MDR report key: 4911620 · Received June 26, 2015

    Report

    Report Number
    4911620
    Event Type
    Malfunction
    Date Received
    June 26, 2015
    Date of Event
    June 10, 2015
    Report Date
    June 26, 2015
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MI, US

    Narratives

    Description of Event or Problem · 1

    PRIOR TO STARTING A CASE THE OR TABLE WAS LOWERED TO ENABLE THE PATIENT TO MOVE ONTO THE TABLE. BEFORE STARTING THE PROCEDURE THE PHYSICIAN REQUESTED THE TABLE BE HEIGHTENED. AT THIS TIME THE TABLE WOULD NOT RAISE. STAFF WAS UNABLE TO ADJUST THE OR TABLE TO MEET THE DOCTOR'S REQUEST. A TECHNICIAN WAS CALLED INTO THE ROOM TO TROUBLE SHOOT THE ISSUE, BUT THE TABLE CONTINUED TO NOT FUNCTION PROPERLY. THE PHYSICIAN THEN HAD TO MAKE MODIFICATIONS TO CONTINUE THE PROCEDURE. THE TECHNICIAN WAS ABLE TO RESOLVE THE ISSUE AFTER THE CONCLUSION OF THE CASE.

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR