BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SPECTRA WAVEWRITER

    MDR report key: 8182653 · Received December 19, 2018

    Report

    Report Number
    3006630150-2018-62385
    Event Type
    Injury
    Date Received
    December 19, 2018
    Date of Event
    December 5, 2018
    Report Date
    February 26, 2019
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION
    Product Code
    LGW
    UDI-DI
    08714729951254
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 0

    MODEL NUMBER/CATALOG NUMBER: SC-2218-50 SERIAL NUMBER: (B)(4) BATCH/LOT NUMBER : 20958862 / 5030730 MODEL/CATALOG DESCRIPTION: LINEAR ST LEAD KIT 50 CM THE EXPLANTED DEVICES WERE NOT RETURNED TO BSN AS THEY WERE DISCARDED BY THE MEDICAL FACILITY. A REVIEW OF THE MANUFACTURING DOCUMENTATION FOR THE IPG AND LEADS REVEALED THAT NO ANOMALIES OR DEVIATIONS POTENTIALLY RELATE TO THE EVENT OCCURRED DURING MANUFACTURING.

    Description of Event or Problem · 0

    A REPORT WAS RECEIVED THAT THE PATIENTS SKIN AROUND THE IPG SITE WAS NOT HEALING PROPERLY AND THE INCISION CAME OPEN. THE PATIENT WILL UNDERGO AN EXPLANT PROCEDURE.

    Description of Event or Problem · 1

    A REPORT WAS RECEIVED THAT THE PATIENTS AKIN AROUND THE IPG SITE WAS NOT HEALING PROPERLY AND THE INCISION CAME OPEN. THE PATIENT WILL UNDERGO AN EXPLANT PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1020545 SPECTRA WAVEWRITER STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION SC-1160 336317 08714729951254

    Patients

    Seq Age Sex Outcome Treatment
    1 72 YR Required Intervention