Skip to content

Clik™ Anchor SC-4276Recalls & reported problems

Boston Scientific Neuromodulation Corporation · Hex Wrench, 7.6cm · Class 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 08714729791973), received between Jun 18, 2025 and Jun 18, 2025 — 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: 1 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: 0 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

  • Erosion1
  • Pain1

Recent adverse event reports

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

  • InjuryJun 18, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PATIENT WAS EXPERIENCING PAIN AT THE MIDLINE INCISION OVER THE ANCHOR SITES AND WORSEN WHEN LEANING. THE PATIENT'S CLICK ANCHOR WAS ERODING AND POKING WITH A SMALL OPENING TO THE SKIN CAUSING SORENESS WITH A LOT OF PRESSURE. IN ADDITION, THE ANCHOR SITE WAS TENDER AND PALPABLE TO TOUCH. THE PATIENT UNDERWENT A PROCEDURE WHEREIN THE PATIENT'S CLICK ANCHOR WAS BURIED DEEPER AND THE PATIENT WAS DOING WELL POSTOPERATIVELY.

    Patient problems: Erosion; Pain

    MAUDE report 22276598 ↗

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-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-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-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-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-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 PAIN RELIEF devices

All STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page