BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RETROBULBAR NEEDLE

    MDR report key: 20064 · Received January 27, 1995

    Report

    Report Number
    20064
    Event Type
    Injury
    Date Received
    January 27, 1995
    Date of Event
    January 27, 1995
    Report Date
    January 27, 1995
    Manufacturer
    HI-LINE MEDICAL
    Product Code
    FMF
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    CA, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    A RETROBULBAR HEMORRHAGE OCCURRED WHEN THE RETROBULBAR INJECTION WAS GIVEN. A SHARP EDGE WAS NOTICED ON THE TIP OF THE NEEDLE USED FOR THE INJECTION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RETROBULBAR NEEDLE RETROBULBAR NEEDLE FMF HI-LINE MEDICAL 23GX1.50" ATKINSON 12926026

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR Hospitalization