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WaveWriter Alpha™ SC-6500-72Recalls & reported problems

Boston Scientific Neuromodulation Corporation · Patient Trial Kit · Class 3

All models of WaveWriter Alpha (3)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 08714729995241), received between Sep 22, 2026 and Sep 22, 2026 — classified as 1 injury.

17 other recalls cover devices cleared under the same FDA submission (P030017); they may or may not involve this specific model.

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 1 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Inappropriate Device Stimulation of Tissue1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjurySep 22, 2026Adverse Event Without Identified Device or Use Problem

    It was reported that the patient was experiencing device shocking during trail period.

    Patient problems: Inappropriate Device Stimulation of Tissue

    MAUDE report 50857808 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P030017. One submission often covers many models, so check the product and lot details in each record.

  • Z-2879-2026 · Jun 17, 2026 · Open, Classified
    INFINION CX LEAD KIT, 50CM, Model: SC-2317-50, Material: M365SC2317500; INFINION CX LEAD KIT, 70CM, Model: SC-2317-70, Material: M365SC2317700. part of the Boston Scientific Spin
  • Z-2404-2026 · Apr 29, 2026 · Open, Classified
    Boston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
  • Z-2617-2024 · Jul 17, 2024 · Open, Classified
    WAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320
  • Z-2124-2020 · Apr 24, 2019 · Terminated
    Fifty-five (55) cm 8 Contact Extension Kit, part number M365SC3138550 - Product Usage: Lead Extensions are designed to connect the percutaneous leads to the Implantable Pulse Gene
  • Z-2121-2020 · Apr 24, 2019 · Terminated
    LinearTM 3-4 50 cm 8 Contact Lead Kit, part number M365SC2352500. Leads function as a component of Boston Scientific's Spinal Cord Stimulation (SCS) systems by delivering electric
  • Z-2122-2020 · Apr 24, 2019 · Terminated
    The LinearTM 3-4 70 cm 8 Contact Lead Kit, part number M365SC2352700 is part of a spinal cord stimulation system for prescription use only as an aid in the management of chronic i
  • Z-2120-2020 · Apr 24, 2019 · Terminated
    Thirty-five (35) cm 8 Contact Extension Kit, part number M365SC3138350. Package Contents: Lead Extension Kit (1) Lead Extension (1) Hex Wrench (1) Tunneling Tool Assembly (1) Devic
  • Z-2123-2020 · Apr 24, 2019 · Terminated
    Precision TM M8 Adapter, 15 cm, part number M365SC9218150 - Product Usage: The adapter is part of a spinal cord stimulation system for prescription use only indicated as an aid in
  • Z-2119-2020 · Apr 24, 2019 · Terminated
    ArtisanTM 70 cm 2 x 8 Surgical Lead Kit, part number M365SC8216700. 2 x 8 Surgical Paddle Lead Kit: (1) One Paddle Lead (4); Four Suture Sleeves; (2) Lead Position Labels, left
  • Z-1409-2010 · Mar 19, 2010 · Terminated
    Bionic NAVIGATOR Clinician Programmer Model Number SC-7150-4
  • Z-0271-2009 · Sep 22, 2008 · Terminated
    Precision Charger 1.0 (Model Number SC-5300) for the Precision Spinal Cord Stimulator System labeled as BIONICS SCS-CHARGING KIT CONTENTS Charger (1) Base Station (1) Belt Po
  • Z-1441-2012 · Apr 22, 2008 · Terminated
    OMG (Observational Mechanical Gateway) Connector - A Model Number SC-9305 The Precision Spinal Cord Stimulator System is indicated as an aid in the management of chronic intractabl
  • Z-0960-2008 · Oct 5, 2007 · Terminated
    Advanced Bionics Precision Implantable Pulse Generator Kit, Model Number: SC-1110 with firmware version prior to Revision 3.02, Advanced Bionics Corportation, Sylmar, CA 91342
  • Z-0055-2008 · Aug 3, 2007 · Terminated
    Precision Implantable Pulse Generator (IPG), Model Number SC-110
  • Z-0700-2007 · Jan 30, 2007 · Terminated
    The Precision Implantable Pulse Generator, Model Number SC-1110

…and 2 more.

Other Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy devices

All Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy devices →

Sources and updates

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