BEUDAMED
    FDA Adverse Event Summary report: N

    30328 13GAX2IN BN NARROW SNARECOIL NDL

    MDR report key: 589884 · Received April 7, 2005

    Report

    Report Number
    1282497-2005-00005
    Date Received
    April 7, 2005
    Report Date
    April 6, 2005
    Manufacturer
    RANFAC
    Product Code
    LWE
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MD, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    A CUSTOMER HAD A PROBLEM WITH THE BN MARROW SNARECOIL NDL . THE CUSTOMER STATES "NEEDLE SNAPPED IN HALF AND PLASTIC HUB SEPARATED FROM NEEDLE CAUSING NEEDLE PORTION TO REMAIN IN PATIENT. DOCTOR WAS ABLE TO REMOVE A PIECE BUT HAS TO SCHEDULE SURGERY TO REMOVE REMAINING PIECE. INJECTION WAS ON THE RIGHT POSTERIAL ILICA BONE."

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 30328 13GAX2IN BN NARROW SNARECOIL NDL BONE MARROW NEEDLE LWE RANFAC SC2013X 10017

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN