BEUDAMED
    FDA Adverse Event Other Summary report: N

    J NEEDLE 8G X 4"

    MDR report key: 366514 · Received December 5, 2001

    Report

    Report Number
    1213649-2001-00001
    Event Type
    Other
    Date Received
    December 5, 2001
    Date of Event
    November 6, 2001
    Report Date
    December 5, 2001
    Manufacturer
    POPPER PRECISION INSTRUMENTS
    Product Code
    GDM
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    CANNULA SEPARATED FROM HANDLE ASSY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    54748 J NEEDLE 8G X 4" REUSABLE BONE MARROW BIOPSY NEEDLE GDM POPPER PRECISION INSTRUMENTS NA 1B 5974I

    Patients

    Seq Age Sex Outcome Treatment
    1 29 YR Other