BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PRECISION

    MDR report key: 11905145 · Received May 28, 2021

    Report

    Report Number
    3006630150-2021-02518
    Event Type
    Injury
    Date Received
    May 28, 2021
    Date of Event
    May 7, 2011
    Report Date
    May 28, 2021
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    UDI-DI
    08714729767688
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    DATE OF EVENT: EXACT DATE UNKNOWN, EVENT OCCURRED 10 YEARS AGO. EXPLANT DATE: 10 YEARS AGO. ADDITIONAL SUSPECT MEDICAL DEVICE COMPONENTS INVOLVED IN THE EVENT: PRODUCT FAMILY: SCS-LINEAR LEADS UPN: (B)(4). MODEL: SC-2208-50 SERIAL: (B)(4). BATCH: 203289/203802.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT UNDERWENT AN EXPLANT PROCEDURE FOR AN UNKNOWN REASON. NO FURTHER INFORMATION COULD BE OBTAINED DESPITE GOOD FAITH EFFORTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    798595 PRECISION STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION SC-1110-02 180564 08714729767688

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Required Intervention