BEUDAMED
    FDA Adverse Event Other Summary report: N

    STERIS C-MAX 110

    MDR report key: 3001670 · Received March 8, 2013

    Report

    Report Number
    MW5029314
    Event Type
    Other
    Date Received
    March 8, 2013
    Date of Event
    February 19, 2013
    Report Date
    February 27, 2013
    Manufacturer
    STERIS CORP
    Product Code
    FQO
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    AT APPROX 0855, THE PAGE OPERATOR ANNOUNCED FIRE ALARM IN L&D/MATERNITY AREA. SOURCE IDENTIFIED AS WIRING AT BASED OF BED CAUSING FIRE. AT THE TIME THERE WERE NO PTS IN ANY OF THE 3 OPERATING ROOMS. STAFF DISCOVERED HEAVY SMOKE COMING THROUGH THE CEILING OF OPERATING ROOM 3. SECURITY AND MAINTENANCE CREW RESPONDED, AND (B)(6) FIRE DEPARTMENT CREW RESPONDED SHORTLY AFTER. (B)(6) AND PT SAFETY OFFICER WERE AT THE SCENE INSPECTING FOR THE SOURCE FOR FIRE. A TOTAL OF 7 PTS WERE MOVED TO ANOTHER AREA TO ENSURE SAFETY. THERE WERE NO KNOWN ADVERSE EFFECTS TO PTS AND/OR EMPLOYEES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    99867 STERIS C-MAX 110 SURGICAL TABLE FQO STERIS CORP C-MAX NA

    Patients

    Seq Age Sex Outcome Treatment
    1