BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HYPODERMIC NEEDLES (MONOJECT)

    MDR report key: 273284 · Received April 7, 2000

    Report

    Report Number
    1017768-2000-00004
    Event Type
    Malfunction
    Date Received
    April 7, 2000
    Date of Event
    February 1, 2000
    Report Date
    April 7, 2000
    Manufacturer
    THE KENDALL CO.
    Product Code
    GAA
    Report Source
    Manufacturer report

    Narratives

    Description of Event or Problem · 1

    REC'D MED-WATCH #MW1018067 ON MARCH, 7 2000.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HYPODERMIC NEEDLES (MONOJECT) HYPODERMIC NEEDLE GAA THE KENDALL CO. UNK

    Patients

    Seq Age Sex Outcome Treatment
    1