BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRECISION

    MDR report key: 1021218 · Received March 28, 2008

    Report

    Report Number
    2029203-2008-00188
    Event Type
    Injury
    Date Received
    March 28, 2008
    Date of Event
    March 6, 2008
    Report Date
    March 6, 2008
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
    Product Code
    LGW
    PMA / PMN Number
    P030017
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    THE PATIENT REPORTED RECEIVING A BURN FROM HIS CHARGER. THE PHYSICIAN TREATED THE BURN WITH A TOPICAL OINTMENT. THE PATIENT IS REPORTEDLY DOING WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PRECISION SPINAL CORD STIMULATOR CHARGER LGW BOSTON SCIENTIFIC NEUROMODULATION CORPORATION SC-5300 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention