BEUDAMED
    FDA Adverse Event Injury Summary report: N

    WAVEWRITER ALPHA?

    MDR report key: 24613070 · Received March 16, 2026

    Report

    Report Number
    3006630150-2026-01535
    Event Type
    Injury
    Date Received
    March 16, 2026
    Date of Event
    February 20, 2026
    Report Date
    May 15, 2026
    Manufacturer
    BOSTON SCIENTIFIC NEUROMODULATION CORPORATION
    Product Code
    LGW
    UDI-DI
    08714729985099
    PMA / PMN Number
    P030017
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    PHYSICIAN
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    BLOCK B3: APPROXIMATED BASED ON THE DATE THE MANUFACTURER BECAME AWARE OF THE EVENT. ADDITIONAL SUSPECT MEDICAL DEVICE COMPONENTS INVOLVED IN THE EVENT: MODEL NUMBER/CATALOG NUMBER: SC-2366-70, SERIAL NUMBER: (B)(6), BATCH/LOT NUMBER: 7073369 / 7070925 / 7070937 / 7071020, MODEL/CATALOG DESCRIPTION: LINEAR 3-6 LEAD 70 CM, UNIQUE IDENTIFIER (UDI) #: (B)(4).

    Description of Event or Problem · 0

    IT WAS REPORTED THAT THE PATIENT DEVELOPED AN INFECTION AT THE IMPLANTABLE PULSE GENERATOR (IPG) AND LEAD SITE. THE PATIENT WAS PRESCRIBED WITH ANTIBIOTICS, AND THE WOUND SITE WAS CLEAN UP HOWEVER IT WAS UNSUCCESSFUL IN TENDING THE INFECTION. NO DEVICE MALFUNCTION WAS SUSPECTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    157355 WAVEWRITER ALPHA? STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF LGW BOSTON SCIENTIFIC NEUROMODULATION CORPORATION SC-1232 542672 08714729985099

    Patients

    Seq Age Sex Outcome Treatment
    1 52 YR Male Required Intervention