BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2183613-1999-00015

    MDR report key: 265353 · Received September 8, 1999

    Report

    Report Number
    2183613-1999-00015
    Event Type
    Injury
    Date Received
    September 8, 1999
    Removal / Correction Number
    NI
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    NO INFORMATION

    Narratives

    Description of Event or Problem · 1

    CLINICIANS OBSERVED ECTOPY. WHEN PACEMAKER WAS SHUT OFF, PT RESUMED NORMAL RHYTHM. PACEMAKER BELIEVED TO HAVE CAUSED ECTOPY AND SUBSEQUENT V-FIB.

    Patients

    Seq Age Sex Outcome Treatment
    1 000 Other 5433V INSTRUMENT CABLE