BEUDAMED
    FDA Adverse Event Summary report: N

    MANAN J-TYPE BONE MARROW BIOPSY NEEDLE

    MDR report key: 35296 · Received July 1, 1996

    Report

    Report Number
    35296
    Date Received
    July 1, 1996
    Date of Event
    December 12, 1995
    Report Date
    January 3, 1996
    Manufacturer
    MANAN MEDICAL PRODUCTS, INC.
    Product Code
    KNW
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    BONE MARROW BIOPSY NEEDLE BROKE OFF DURING PROCEDURE. RETAINED NEEDLE FRAGMENT LEFT IN PT. PT BEING OBSERVED POST X-RAY EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MANAN J-TYPE BONE MARROW BIOPSY NEEDLE J-TYPE BONE MARROW BIOPSY NEEDLE KNW MANAN MEDICAL PRODUCTS, INC. M092995

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR