BEUDAMED
    FDA Adverse Event Injury Summary report: N

    QUATTRODE

    MDR report key: 2864418 · Received December 6, 2012

    Report

    Report Number
    1627487-2012-06867
    Event Type
    Injury
    Date Received
    December 6, 2012
    Date of Event
    November 13, 2012
    Report Date
    November 13, 2012
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    GZB
    PMA / PMN Number
    K072462
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SJM HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    DEVICE 1 OF 3. REFERENCE MFR. REPORT: 1627487-2012-06868, 06869. THE PATIENT HAS THREE LEADS (FOR OFF-LABEL USE). IT WAS REPORTED THE PATIENT WAS EXPERIENCING PAIN AT THE LEAD SITE. AS A RESULT, TWO OF THE LEADS WERE REPOSITIONED ON (B)(6) 2012. REPOSITIONING THE LEADS RESOLVED THE PATIENT'S ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 QUATTRODE SCS LEAD GZB ST. JUDE MEDICAL - NEUROMODULATION 3169 3546969

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Required Intervention SCS EXTENSIONS: MODEL: 3346 (2)| IMPLANT:| SCS IPG: MODEL 3716| IMPLANT: