Quattrode™ 3156 (UDI 05414734406079)Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 05414734406079), received between Dec 20, 2018 and Aug 31, 2026 — classified as 4 injuries.

The most frequently reported specific device problem is “High impedance” (2 reports).

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

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryAug 31, 2026High impedance

  It was reported that the patient's leads exhibited high impedances. As a result, surgical intervention may be undertaken to address the issue. It is unknown which lead exhibited the high impedances

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50532528 ↗
• InjuryDec 6, 2019High impedance; High impedance

  IT WAS REPORTED THAT THE PATIENT UNDERWENT SURGICAL INTERVENTION ON (B)(6) 2020 WHEREIN THE PATIENT HAD THEIR LEADS AND IPG EXPLANTED AND REPLACED. THERAPY HAS BEEN RESTORED POST-OP.

  Patient problems: Inadequate Pain Relief

  MAUDE report 9427004 ↗
• InjuryDec 26, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DEVICE 2 OF 3. REFERENCE MFR. REPORT: 1627487-2018-13000. REFERENCE MFR. REPORT: 1627487-2018-13002. IT WAS REPORTED THE PATIENT SUFFERED A FALL AND THEN EXPERIENCED INEFFECTIVE STIMULATION. O ADDRESS THE ISSUE, THE PHYSICIAN EXPLANTED AND REPLACED THE PATIENT¿S THREE LEADS. POSTOPERATIVELY, EFFECTIVE THERAPY WAS RESTORED.

  Patient problems: Fall; Inadequate Pain Relief

  MAUDE report 8197121 ↗
• InjuryDec 20, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  DEVICE 1 OF 3: REFERENCE MFR. REPORT: 1627487-2018-13000, REFERENCE MFR. REPORT: 1627487-2018-13001, REFERENCE MFR. REPORT: 1627487-2018-13002. IT WAS REPORTED THE PATIENT SUFFERED A FALL AND THEN EXPERIENCED INEFFECTIVE STIMULATION. TO ADDRESS THE ISSUE, THE PHYSICIAN EXPLANTED AND REPLACED THE PATIENT¿S THREE LEADS. POSTOPERATIVELY, EFFECTIVE THERAPY WAS RESTORED.

  Patient problems: Fall; Inadequate Pain Relief

  MAUDE report 8185156 ↗

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-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-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-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-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-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-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-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-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