BEUDAMED
    FDA Adverse Event Death Summary report: N

    NEPHROMAX¿

    MDR report key: 2894061 · Received January 3, 2013

    Report

    Report Number
    3005099803-2013-00014
    Event Type
    Death
    Date Received
    January 3, 2013
    Date of Event
    December 7, 2012
    Report Date
    December 7, 2012
    Manufacturer
    BOSTON SCIENTIFIC - GALWAY
    Product Code
    LJE
    PMA / PMN Number
    K952968
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    NOTE: THIS REPORT IS FOR ONE OF ELEVEN BOSTON SCIENTIFIC CORPORATION (BSC) DEVICES USED DURING THIS PROCEDURE. PLEASE REFERENCE MDR# 3005099803-2012-06224 FOR THE PARENT DEVICE. IT WAS REPORTED TO BSC THAT A NEPHROMAX BALLOON DILATATION CATHETER WAS USED IN A PERCUTANEOUS NEPHROLITHOTOMY (PCNL) PERFORMED ON (B)(6) 2012. DURING THE PROCEDURE, THE PHYSICIAN NOTED THAT THE PATIENT'S BLOOD PRESSURE DROPPED SUDDENLY. SHE BLED "PROFUSELY". THE PATIENT, WHOSE AGE WAS REPORTED TO BE (B)(6), HAD OTHER CO-MORBIDITIES (SPECIFICS UNKNOWN). SHE DIED THE FOLLOWING DAY, (B)(6) 2012. THERE WERE NO REPORTED DEFECTS OR MALFUNCTIONS WITH THE BSC DEVICE. THE PHYSICIAN HAS NOT RESPONDED TO SEVERAL REQUESTS FOR ADDITIONAL INFORMATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    3626 NEPHROMAX¿ CATHETER, NEPHROSTOMY LJE BOSTON SCIENTIFIC - GALWAY M0062101440

    Patients

    Seq Age Sex Outcome Treatment
    1 Death