BEUDAMED
    FDA Adverse Event Injury Summary report: N

    U OF I STERNUM NEEDLE 15GA

    MDR report key: 291105 · Received August 18, 2000

    Report

    Report Number
    1423507-2000-00213
    Event Type
    Injury
    Date Received
    August 18, 2000
    Report Date
    August 18, 2000
    Manufacturer
    ALLEGIANCE HEALTHCARE CORPORATION
    Product Code
    FMI
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    NEEDLE BROKE INTO PATIENT DURING USE. NEEDLE WAS SUCCESSFULLY RETRIEVED WITH FORCEPS. RETRIVAL OF NEEDLE WAS PAINFUL PROCESS FOR PT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 U OF I STERNUM NEEDLE 15GA NEEDLE FMI ALLEGIANCE HEALTHCARE CORPORATION SU21000 UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN Other