BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2183613-1999-00011

    MDR report key: 265539 · Received September 8, 1999

    Report

    Report Number
    2183613-1999-00011
    Event Type
    Injury
    Date Received
    September 8, 1999
    Date of Event
    May 30, 1999
    Report Date
    June 4, 1999
    Removal / Correction Number
    NI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    I

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR Life Threatening