BEUDAMED
    FDA Adverse Event Death Summary report: N

    KANEDA

    MDR report key: 14616 · Received March 23, 1994

    Report

    Report Number
    14616
    Event Type
    Death
    Date Received
    March 23, 1994
    Report Date
    March 21, 1994
    Manufacturer
    ACROMED CORP.
    Product Code
    MCV
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    MD, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    MIGRATION AND LACERATION OF DEVICE. PT HAD BLEEDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KANEDA Implant ANTERIOR SPINAL INSTRUMENTATION DEVICE MCV ACROMED CORP. UNKNOWN UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR Death