BEUDAMED
    FDA Adverse Event Injury Summary report: N

    CURRENT PLUS DR, SJ4 CONNECTOR

    MDR report key: 1831131 · Received September 10, 2010

    Report

    Report Number
    2017865-2010-03577
    Event Type
    Injury
    Date Received
    September 10, 2010
    Date of Event
    March 15, 2010
    Manufacturer
    ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
    Product Code
    LWS
    PMA / PMN Number
    PMAP910023
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    ALL INFORMATION PROVIDED BY MANUFACTURER, NO MEDWATCH FORM WAS RECEIVED. REVIEW OF QUALITY RECORDS. LATE DUE TO DELAY IN RECEIVING PAPERWORK.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT NOTICED REDNESS AT THE LATERAL INCISION EDGE ALONG THE LATERAL DEVICE EDGE. HE WAS THEN STARTED ON KEFLEX BUT THEN DEVELOPED BLISTERS AT THE INCISION SITE. HE WAS ADMITTED TO THE HOSPITAL AND THE SYSTEM WAS EXPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 CURRENT PLUS DR, SJ4 CONNECTOR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR LWS ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION CD2211-36Q NA

    Patients

    Seq Age Sex Outcome Treatment
    1 38 YR Required Intervention 7120Q/58, (B)(4), 1699TC/46, (B)(4)