BEUDAMED
    FDA Adverse Event Other Summary report: N

    JAMSHIDI (TJ) BONE MARROW BIOPSY/ASP NDL

    MDR report key: 564389 · Received January 10, 2005

    Report

    Report Number
    1423507-2005-00002
    Event Type
    Other
    Date Received
    January 10, 2005
    Date of Event
    December 8, 2004
    Report Date
    January 10, 2005
    Manufacturer
    CARDINAL HEALTH
    Product Code
    FCG
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    DURING BIOPSY, WHILE REMOVING THE DEVICE, THE NEEDLE BROKE AT 1/3 FROM THE TOP. PT HAD TO UNDERGO SURGERY TO REMOVE THE REMAINING PIECE OF THE NEEDLE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JAMSHIDI (TJ) BONE MARROW BIOPSY/ASP NDL BONE MARROW BIOPSY NEEDLE FCG CARDINAL HEALTH TJC4008 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other