BEUDAMED
    FDA Adverse Event Other Summary report: N

    BIOPSY NEEDLE

    MDR report key: 18680 · Received January 3, 1995

    Report

    Report Number
    MW1004632
    Event Type
    Other
    Date Received
    January 3, 1995
    Date of Event
    December 1, 1994
    Report Date
    December 15, 1994
    Manufacturer
    C.R. BARD, INC.
    Product Code
    GAA
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KY, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    A 14 GAUGE CORE NEEDLE WAS USED DURING BIOPSY. ON THE SPECIMEN RADIOGRAPH, SEVERAL METALLIC FILINGS WERE SEEN. ON VISUAL EXAMINATION OF THE NEEDLE, NO APPARENT DAMAGE WAS SEEN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BIOPSY NEEDLE CORE NEEDLE GAA C.R. BARD, INC. 03GES029

    Patients

    Seq Age Sex Outcome Treatment
    1 44 YR Other