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A127™ 2343Recalls & reported problems

St. Jude Medical, Inc. · Extension, 60cm · Class 3 · Implant

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05414734401432), received between Nov 9, 2018 and Jun 23, 2023 — classified as 2 injuries.

The most frequently reported specific device problem is “Failure to Deliver Energy” (1 report).

14 other recalls cover devices cleared under the same FDA submission (P010032); 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.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Failure to Deliver Energy1

Patient problems

  • Inadequate Pain Relief1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryJun 23, 2023Failure to Deliver Energy; Failure to Deliver Energy

    IT WAS REPORTED THE PATIENT WAS EXPERIENCING INEFFECTIVE STIMULATION DUE TO AUTO REDUCING. SURGICAL INTERVENTION TOOK PLACE WHEREIN THE EXTENSION WAS EXPLANTED AND REPLACED. STIMULATION WAS RESTORED.

    Patient problems: Inadequate Pain Relief

    MAUDE report 17192261 ↗
  • InjuryNov 9, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THE PATIENT WAS SCHEDULED FOR IPG REPLACEMENT ON (B)(6) 2018. IT WAS DECIDED NOT TO ATTEMPT TO FIND THE LEAD/EXTENSION SITE DUE TO PATIENT DISCOMFORT AND RISKS WITH CONTINUED SEDATION. AS A RESULT, THE PROCEDURE WAS ABANDONED AND THE IPG WAS EXPLANTED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8056751 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under P010032. One submission often covers many models, so check the product and lot details in each record.

  • Z-0458-2026 · Oct 6, 2025 · Open, Classified
    Eterna SCS IPG (Implantable Pulse Generator), Model Number 32400
  • Z-2511-2023 · Jul 18, 2023 · Open, Classified
    Infinity 7 Implantable Pulse Generator REF 6662 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensio
  • Z-2507-2023 · Jul 18, 2023 · Open, Classified
    Proclaim Plus 5 Implantable Pulse Generator REF 3670 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more ext
  • Z-2506-2023 · Jul 18, 2023 · Open, Classified
    Proclaim" XR 7 Implantable Pulse Generator REF 3662 (previously known as Proclaim" 7 Elite IPG) Product Description: The implantable pulse generator (IPG) is an electronic device
  • Z-2509-2023 · Jul 18, 2023 · Open, Classified
    Proclaim DRG Implantable Pulse Generator REF 3664 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extens
  • Z-2510-2023 · Jul 18, 2023 · Open, Classified
    Infinity 5 Implantable Pulse Generator REF 6660 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more extensio
  • Z-2505-2023 · Jul 18, 2023 · Open, Classified
    Proclaim XR 5 Implantable Pulse Genterator REF 3660 (previously known as Proclaim" 5 Elite IPG) Model 3660 Product Description: The implantable pulse generator (IPG) is an electr
  • Z-2508-2023 · Jul 18, 2023 · Open, Classified
    Proclaim Plus 7 Implantable Pulse Generator REF 3672 Product Description: The implantable pulse generator (IPG) is an electronic device designed to be connected to one or more ext
  • Z-2692-2017 · Jun 2, 2017 · Terminated
    Proclaim 7 Elite, Implantable Pulse Generator, REF 3662, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be c
  • Z-2691-2017 · Jun 2, 2017 · Terminated
    Proclaim 5 Elite, implantable Pulse Generator, REF 3660, Rx only, STERILE EO Product Usage: The Proclaim implantable pulse generator (IPG) is an electronic device designed to be c
  • Z-1785-2013 · Nov 30, 2012 · Terminated
    Eon and Eon Mini charging system, model numbers Eon -3701 (Wall Charger), 3711 (Portable Charger) and Eon Mini -3721 (Charger); This is a continuation of the firm's July 2012 reca
  • Z-0025-2013 · Sep 4, 2012 · Terminated
    The Eon Mini Implantable Pulse Generator (IPG) is a 16-channel, rechargeable, multi-program system that allows the connection of one or two leads with four, eight, and 16 electrode
  • Z-1738-2013 · Jul 26, 2012 · Terminated
    Eon - 3701 (Wall Charger) and 3711 (Portable Charger). Product Usage: Eon: Eon system is indicated as an aid in the management of chronic intractable pain of the trunk and/or li
  • Z-3091-2011 · Jun 2, 2009 · Terminated
    Software version 3.3 for Rapid Programmer devices, Model 3832. Software version 3.3 for Rapid Programmer devices, a personal digital assistant (PDA) based programmer supporting im

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Sources and updates

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