BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HYPODERMIC NEEDLE

    MDR report key: 2010425 · Received March 4, 2011

    Report

    Report Number
    MW5019654
    Event Type
    Injury
    Date Received
    March 4, 2011
    Date of Event
    March 4, 2011
    Report Date
    March 4, 2011
    Product Code
    FMI
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    (B)(6) HOSPITAL IS GIVING MEDICATIONS WITH DIRTY NEEDLES. AFTER RECEIVING AN INJECTION IN PELVIC AREA, PT IS HAVING PAIN IN OVARIES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HYPODERMIC NEEDLE FMI

    Patients

    Seq Age Sex Outcome Treatment
    1