BEUDAMED
    FDA Adverse Event Summary report: N

    30328 11GX6IN BN MARR SNARECOIL NDLE

    MDR report key: 558903 · Received May 8, 2004

    Report

    Report Number
    1282497-2004-00012
    Date Received
    May 8, 2004
    Report Date
    April 9, 2004
    Manufacturer
    RANFAC CORPORATION
    Product Code
    LWE
    Report Source
    Manufacturer report
    Reporter Location
    GA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED TO TYCOHEALTHCARE KENDALL THAT DURING A BONE MARROW BIOPSY THE NEEDLE SHAFT BROKE. THE DOCTOR HAD TO REMOVE THE NEEDLE WITH A PAIR OF PLIERS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 30328 11GX6IN BN MARR SNARECOIL NDLE BONE MARROW BIOPSY NEEDLE LWE RANFAC CORPORATION * UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other