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
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, ClassifiedINFINION 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, ClassifiedBoston Scientific Model SC-4318, Clik X Anchor REF: M365SC43180
- Z-2617-2024 · Jul 17, 2024 · Open, ClassifiedWAVEWRITER ALPHA: Model: SC-1216, 16 IPG KIT, REF: M365SC12160; Model: SC-1232, 32 IPG KIT, REF: M365SC12320
- Z-2124-2020 · Apr 24, 2019 · TerminatedFifty-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 · TerminatedLinearTM 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 · TerminatedThe 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 · TerminatedThirty-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 · TerminatedPrecision 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 · TerminatedArtisanTM 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 · TerminatedBionic NAVIGATOR Clinician Programmer Model Number SC-7150-4
- Z-0271-2009 · Sep 22, 2008 · TerminatedPrecision 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 · TerminatedOMG (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 · TerminatedAdvanced 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 · TerminatedPrecision Implantable Pulse Generator (IPG), Model Number SC-110
- Z-0700-2007 · Jan 30, 2007 · TerminatedThe 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
- Intellis™ 97716Medtronic, Inc. · Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy1,125 reports
- WaveWriter Alpha™ Prime SC-1432Boston Scientific Neuromodulation Corporation · Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy7 deaths971 reports
- WaveWriter Alpha™ Prime 16 SC-1416Boston Scientific Neuromodulation Corporation · Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy12 deaths911 reports
- Intellis™ 97716Medtronic, Inc. · Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy635 reports
- Intellis™ Pro 977118Medtronic, Inc. · Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy201 reports
- Vectris™ SureScan® 977A260Medtronic, Inc. · Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy71 reports
- N/A A710Medtronic, Inc. · Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy1 recall0 reports
- Infinion™ Pro SC-2318-50Boston Scientific Neuromodulation Corporation · Stimulator, spinal-cord, totally implanted for relief of pain due to diabetic neuropathy41 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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