BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ROSENTHAL NEEDLE 16G X 2"

    MDR report key: 285518 · Received June 16, 2000

    Report

    Report Number
    2414164-2000-00001
    Event Type
    Malfunction
    Date Received
    June 16, 2000
    Date of Event
    May 25, 2000
    Report Date
    June 16, 2000
    Manufacturer
    POPPER PRECISION INSTRUMENTS
    Product Code
    DWO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    NEEDLE CAME APART DURING USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ROSENTHAL NEEDLE 16G X 2" REUSABLE BONE MARROW BIOPSY NEEDLE DWO POPPER PRECISION INSTRUMENTS NA 9D 2469

    Patients

    Seq Age Sex Outcome Treatment
    1 * Other