BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRECISION®

    MDR report key: 2072091 · Received April 28, 2011

    Report

    Report Number
    3006630150-2011-00624
    Event Type
    Injury
    Date Received
    April 28, 2011
    Date of Event
    February 24, 2011
    Report Date
    April 4, 2011
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    HEALTH PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    ADDITIONAL SUSPECT MEDICAL DEVICE COMPONENTS INVOLVED IN THE EVENT: MODEL # SC-2218-50 (B)(4) DESCRIPTION: ST LINEAR LEAD, 50CM WITH PRE-LOADED 0.014 INCH STYLET MODEL # SC-1110-02 (B)(4) DESCRIPTION: IPG KIT (WITHOUT PULL-THROUGH TUNNELER) THE EXPLANTED DEVICES WERE NOT RETURNED TO BSN AS THEY WERE DISCARDED BY THE MEDICAL FACILITY.

    Additional Manufacturer Narrative · 1

    INFORMATION PROVIDED. A REVIEW OF THE MANUFACTURING DOCUMENTATION FOR THE LEADS AND IPG REVEALED THAT NO ANOMALIES OR DEVIATIONS POTENTIALLY RELATED TO THE EVENT OCCURRED DURING MANUFACTURING. A REVIEW OF THE STERILIZATION DOCUMENTATION FOR THE LEADS AND IPG FOUND THEM TO BE SATISFACTORY.

    Description of Event or Problem · 1

    A REPORT WAS RECEIVED THAT FOLLOWING THE NON-DEVICE RELATED EXPLANT OF THE PATIENT'S PRECISION SYSTEM THE PATIENT DEVELOPED AN INFECTION. THE PATIENT'S SYMPTOM INCLUDED DISCHARGE FROM THE LEAD SITE. THE PHYSICIAN DOES NOT BELIEVE THE INFECTION WAS DEVICE OR PROCEDURE RELATED. THE PATIENT WAS GIVEN ORAL ANTIBIOTICS AND WAS REPORTEDLY DOING WELL.

    Description of Event or Problem · 1

    A REPORT WAS RECEIVED THAT FOLLOWING THE NON-DEVICE RELATED EXPLANT OF THE PATIENT'S PRECISION SYSTEM THE PATIENT DEVELOPED AN INFECTION. THE PATIENT'S SYMPTOM INCLUDED DISCHARGE FROM THE LEAD SITE. THE PHYSICIAN DOES NOT BELIEVE THE INFECTION WAS DEVICE OR PROCEDURE RELATED. THE PATIENT WAS GIVEN ORAL ANTIBIOTICS AND WAS REPORTEDLY DOING WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRECISION® SPINAL CORD STIMULATOR LGW BOSTON SCIENTIFIC NEUROMODULATION SC-2218-50 N/A

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Required Intervention