BEUDAMED
    FDA Adverse Event Other Summary report: N

    POWER MORCELLATOR

    MDR report key: 4352662 · Received December 14, 2014

    Report

    Report Number
    MW5039679
    Event Type
    Other
    Date Received
    December 14, 2014
    Date of Event
    April 8, 2014
    Report Date
    December 14, 2014
    Product Code
    HET
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD A TOTAL HYSTERECTOMY PERFORMED DUE TO FIBROID TUMORS. THE SURGERY WAS AN ABDOMINAL INCISION, NOT LAPAROSCOPIC. THE SURGERY WAS PERFORMED AT (B)(6) BETWEEN 1984 AND 1986 (FORGIVE MY MEMORY). IN (B)(6) 2014, I WAS DIAGNOSED WITH LEIOMYOSARCOMA DETECTED IN THE LOWE LOBE OF MY RIGHT LUNG, MY PHYSICIANS SAID IT WAS RARE FOR THIS TYPE OF CANCER TO ORIGINATE IN THE LUNG. FURTHER TESTS FOUND THAT I HAVE ANOTHER SARCOMA IN MY LEFT FOOT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    819385 POWER MORCELLATOR POWER MORCELLATOR HET

    Patients

    Seq Age Sex Outcome Treatment
    1 66 YR Other