Precision SpectraRecalls & reported problems across all models

We found 3 models of Precision Spectra by Boston Scientific Neuromodulation Corporation in the FDA's device registry (GUDID). Together they are named in 11,348 adverse event reports in the FDA's MAUDE database, received between May 21, 2014 and Sep 30, 2026 — classified as 55 deaths, 10,989 injuries, 304 malfunctions.

The most frequently reported specific device problem is “Charging Problem” (4,520 reports).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works

Most reported Precision Spectra problems

Precision Spectra models

3 models, most reported first. Each model has its own page with its reports, recalls and device details.

• Precision Spectra ™ SC-1132

  STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
  53 deaths11,269 reports
• Precision Spectra™ SC-1032B

  STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
  2 deaths78 reports
• Precision Spectra™ SC-5532-1

  STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF
  1 report

Recent Precision Spectra adverse event reports

The 15 most recent reports across all models, in the reporter's own words as published by the FDA.

• InjurySep 30, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50954807 ↗
• InjurySep 30, 2026Nonstandard Device; Unexpected Therapeutic Results; Charging Problem

  Patient problems: Pain

  MAUDE report 50947455 ↗
• InjurySep 29, 2026Power Problem; Wireless Communication Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50941035 ↗
• InjurySep 29, 2026Unexpected Therapeutic Results; Battery Problem

  It was reported that the patient was experiencing loss of stimulation. It was also noted that the patients implantable pulse generator (IPG) was nearing end of battery life. The patient underwent an IPG replacement procedure and was doing well postoperatively. The explanted device was retained by customer per facility policy.

  Patient problems: Pain

  MAUDE report 50933398 ↗
• InjurySep 28, 2026Inappropriate/Inadequate Shock/Stimulation

  Patient problems: Burning Sensation; Discomfort; Implant Pain; Inappropriate Device Stimulation of Tissue; Swelling/ Edema

  MAUDE report 50926478 ↗
• InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50924197 ↗
• InjurySep 28, 2026Charging Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50915667 ↗
• InjurySep 25, 2026Charging Problem; Wireless Communication Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50903744 ↗
• InjurySep 25, 2026Battery Problem; Charging Problem; Wireless Communication Problem

  It was reported that the patient had difficulty charging the implantable pulse generator (IPG). It was also noted that the patient feels a tingle sensation that is much stronger that her normal. The patient underwent an IPG replacement procedure and was doing well postoperatively. The explanted device was discarded and will not be returned.

  Patient problems: Inappropriate Device Stimulation of Tissue

  MAUDE report 50899033 ↗
• InjurySep 25, 2026Unexpected Therapeutic Results

  It was reported that the patient was experiencing inadequate stimulation. It was also stated that the patient's lead placement was not ideal for the patient's pain pattern. The patient underwent a procedure wherein the implantable pulse generator (IPG) and spinal cord stimulator (SCS) paddle lead were explanted. The patient was doing well postoperatively and the explanted devices were retained by the medical facility and will not be returned.

  Patient problems: Pain

  MAUDE report 50897880 ↗
• InjurySep 25, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that this Spinal Cord Stimulation (SCS) patient underwent an explant procedure due to implantable pulse generator (IPG) becoming nonfunctional. Post operatively the patient is doing well. In accordance with facility policy the explanted device was retained and will not be returned.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50897596 ↗
• InjurySep 24, 2026Unexpected Therapeutic Results; Charging Problem

  It was reported that the patient was unable to receive therapy due to difficulty charging the Implantable Pulse Generator (IPG). The patient underwent an IPG replacement procedure and was doing well postoperatively. The explanted IPG was discarded per hospital policy.

  Patient problems: Pain

  MAUDE report 50877572 ↗
• InjurySep 23, 2026Adverse Event Without Identified Device or Use Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50869254 ↗
• InjurySep 23, 2026Adverse Event Without Identified Device or Use Problem

  It was reported that the patient underwent an explant due to an infection from another procedure.

  Patient problems: Unspecified Infection

  MAUDE report 50867936 ↗
• InjurySep 22, 2026High impedance; Adverse Event Without Identified Device or Use Problem

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50862907 ↗

Other Boston Scientific Neuromodulation Corporation products

• Spectra WaveWriter4 models · 7,251 reports
• Precision17 models · 6,725 reports
• WaveWriter Alpha3 models · 4,356 reports · 1 recall
• Precision Montage MRI2 models · 4,332 reports
• Linear ST5 models · 4,068 reports
• Infinion CX2 models · 2,139 reports · 1 recall
• Superion5 models · 1,488 reports · 2 recalls
• Infinion 165 models · 1,550 reports