“I Could See Metal Through My Skin”: When a Stimulator Battery Breaks Through
Medication, drug and device guides · 13 min read · Published 10 November 2026 · Reviewed 10 November 2026 · Next review May 2027
By Dr Rosemary Listing, PhD (Law) · Medical negligence lawyer since 2014 · Of Counsel, Peter Evans & Associates
Summary
Spinal cord stimulators, including Boston Scientific’s Precision Spectra, have a battery (pulse generator) placed under the skin. Rarely, the skin over it thins, breaks down and the device pushes through. This guide is for people whose stimulator battery became exposed or infected, or whose early warning signs weren’t acted on. It explains why erosion happens, what should be done, and the legal questions.
Quick answer · updated November 2026
Skin erosion over a stimulator battery is rare but serious. Thinning, redness or a shiny patch over the device should be checked promptly, because early problems can sometimes be fixed by adjusting the pocket. Once metal is exposed, the device is usually treated as contaminated and removed. If warning signs were missed or the pocket was too shallow, it is worth having it looked at.
Stimulator battery erosion at a glance
- 1ImplantThe battery sits in a pocket under the skin.
- 2Warning signsThinning, redness, a shiny patch.
- 3Early actionPocket revision may save the device.
- 4Exposed deviceUsually removal of battery and leads.
- 5AfterwardsHealing, then possible re-implantation.
At any stage: a red, hot, leaking wound or fever with a stimulator needs same-day review.
My stimulator had given me my life back after years of leg pain. The battery sat just above my belt line on the left.
About three years in, the skin over it started to look thin and shiny. I mentioned it at a programming appointment. The rep said it looked fine.
Months later it was red and sore. My pain specialist said to stop wearing tight belts.
Then one morning in the shower, I could see a corner of grey metal through my skin.
A composite story, drawn from the experiences of many families I have worked with, combined and changed so that no one can be identified. It does not describe any individual client.
If your stimulator broke through your skin, I want you to know that your questions are reasonable. It is frightening to see a device emerge from your body, and it’s fair to ask whether it could have been prevented or caught earlier.
This guide covers why erosion happens, warning signs, what should be done, records, and how the law looks at it.
Why I can write this
I have been a medical negligence lawyer since 2014 and have worked on many hundreds of claims, including many involving spinal cord stimulators. My doctorate looked at patterns of failure in medical negligence. I am not medically qualified. The clinical facts in this article are checked against named sources, listed in the references, and I explain how I work in our editorial standards.
Start with your question
- Why does a stimulator battery break through the skin?
- What are the warning signs?
- Can it be fixed early?
- What happens if the device is exposed?
- When is it urgent?
- Is it a device or care problem?
- Could this be negligence?
Why erosion happens
A 2021 case report described a stimulator battery extruding through the abdominal wall four years after implantation. The authors listed contributing factors including pressure from a belt, thin fat under the skin, tissue fragility, pockets that are too shallow or the wrong size, and infection.1 They called it a very rare complication.1
Definition
Implantable pulse generator (IPG) is the battery and electronics of a stimulator, placed in a pocket under the skin.
In plain terms: the stimulator’s battery.
Warning signs
Skin that becomes thin, shiny, discoloured or tender over the device, or a device that seems to have moved, should be reviewed by the implanting team, not just the device representative.
Questions to ask
- Is the skin over my battery thinning?
- Has the battery moved?
- Should the pocket be revised before it gets worse?
- Could this be infection?
Early action
The authors note that early erosion without skin breakdown may be managed by surgically revising the pocket, and they recommend monitoring for early skin changes, considering belt lines when placing the pocket, and placing it deep enough.1
When the device is exposed
Once hardware is exposed, it should be assumed to be contaminated, and the authors advise removing the battery and leads, with re-implantation later.1 That means losing pain relief for a period and further surgery.
When it’s urgent
Book a review
- Thin, shiny skin over the device
- The device moving
- Tenderness
In plain terms: see the implanting surgeon soon.
Same day
- Metal visible
- Fluid or pus
- Fever
- Spreading redness
In plain terms: go to your surgeon or emergency today.
Device or care?
Some stimulator problems relate to the device; erosion more often relates to placement, follow-up and response to warning signs. The TGA has reviewed spinal cord stimulators, and you can report problems.2 See our guides to lead migration and headache after a stimulator.
The battery and leads were removed that week. The surgeon said exposed hardware has to come out. I went back to living with the leg pain for six months before a new system went in, deeper this time.
In my records, the programming note said “skin over IPG thin, pt reassured”. The pain clinic letter months later said “erythema over IPG, advise looser clothing”.
Nobody had referred me back to the surgeon.
My partner read the notes in the car. “Two warnings,” he said.
A composite story, drawn from the experiences of many families I have worked with, combined and changed so that no one can be identified. It does not describe any individual client.
What to look for in the records
Your records are often where the story becomes clear. You have a right to access your own health information. In NSW the Health Records and Information Privacy Act 2002 covers both public and private providers, and the Information and Privacy Commission explains how to ask.3 Our step-by-step guide to getting your medical records in Australia walks you through it.
| Record | Why it matters |
|---|---|
| Operation note | Where and how deep the pocket was made. |
| Programming notes | Device rep visits and observations. |
| Clinic letters | What was said about skin changes. |
| Photos | Your own photos of the skin over time. |
| Removal operation note | What was found, including infection. |
| Microbiology | Cultures from the device. |
| Your own diary, photos and messages | Notes made at the time are evidence too. Keep them. |
How the law looks at it
Skin erosion over a stimulator can happen despite good care. The legal questions are whether the pocket was placed appropriately, and whether early warning signs were recognised and acted on.
A claim usually turns on three questions: whether the care fell below what peers would widely accept as competent practice (section 5O of the Civil Liability Act 2002 (NSW))4, whether that shortfall probably caused harm you wouldn't otherwise have had (Tabet v Gett)5, and, where it matters, whether you were told the material risks first (Rogers v Whitaker)67. Our guide to how a medical negligence claim works explains each one in plain terms.
In an erosion case, the questions might be: was the pocket deep enough and placed away from belt lines? Were you told what to watch for? When you reported skin changes, were you referred to the surgeon? Was a pocket revision considered before the device broke through?
In plain terms, the question is whether earlier action would probably have saved the device and avoided removal, lost pain relief and further surgery.
For a stimulator, that would usually include the risks of infection, erosion and further surgery.
Who can claim, and when
The person harmed can claim. In NSW, time usually runs from when you knew, or ought to have known, enough to claim, not from the treatment itself, and courts can sometimes extend it, so an old injury may still count. See time limits in NSW or other states, and ask early.
More: complaint or claim? · how a claim is paid for · what a claim can cover
In my practice
In stimulator files, the device representative’s notes are often important. Skin changes may be noticed at programming visits but not passed to the surgeon. Reading those notes alongside the clinic letters often shows a warning that went nowhere.
Both things can be true
Your stimulator may have changed your life for the better, and the care around it may still have fallen short. Both can be true.
The bigger picture
Spinal cord stimulators have been the subject of a TGA post-market review.2 You can check a practitioner on the Ahpra public register,8 and complaints about care in NSW can go to the Health Care Complaints Commission.9 Our guide to getting your medical records explains how to ask for your file.
Support
You don't have to work through this alone. These services can help:
- Lifeline, 24-hour crisis support: 13 11 14 (listed on healthdirect's helplines page)10
- Beyond Blue, anxiety and depression support: 1300 22 4636
- Medicare Mental Health, help finding mental health support: 1800 595 212
- healthdirect, 24-hour nurse advice: 1800 022 222
- Health Care Complaints Commission (NSW): 1800 043 159
A man who saw metal through his skin now knows it was noticed twice. You deserve that clarity too.
With care,
Rosemary
Frequently asked questions
Why does a stimulator battery break through the skin?
Pressure, thin tissue, a shallow pocket or infection can all contribute.
What are early signs of erosion?
Thin, shiny or red skin over the device, or the device moving.
Can erosion be fixed without removing the device?
Sometimes, if caught early, by revising the pocket.
What happens if the device is exposed?
It is usually removed and replaced later.
Who should I tell about skin changes?
Your implanting surgeon, not only the device representative.
Can I claim for stimulator erosion?
You may well have a claim if placement or follow-up fell short and caused harm.
Questions about your stimulator?
When you're ready, and not before, I can look at what happened and help you understand your options.
Medication, drug and device guides
- Paraquat poisoning and Parkinson’s
- NexGen and Zimmer knee implant failure
- Taxotere (docetaxel) harm
- “I could see metal through my skin”: When a stimulator battery breaks through (you are here)
- Balloon dissector injury in hernia surgery
- Insulin pump failure
Part of our guide to medication, drug and device harm. Not sure where you stand? Try the free claim checker.
References
- Choi E-J, Ri H-S, Park H, et al. Unexpected extrusion of the implantable pulse generator of the spinal cord stimulator: a case report. Anesth Pain Med. 2021;16(1):103–107.
- Therapeutic Goods Administration. Post-market review of spinal cord stimulation (SCS) devices.
- Information and Privacy Commission NSW. Fact sheet: Accessing your health information in NSW.
- Civil Liability Act 2002 (NSW) s 5O, Standard of care for professionals.
- Tabet v Gett [2010] HCA 12.
- Rogers v Whitaker [1992] HCA 58; (1992) 175 CLR 479.
- Australian Commission on Safety and Quality in Health Care. Informed consent.
- Australian Health Practitioner Regulation Agency. Register of practitioners.
- Health Care Complaints Commission NSW. Home page.
- healthdirect Australia. Mental health helplines.
Stories in this article are composites, drawn from the experiences of many families I have worked with, combined and changed so that no one can be identified. They do not describe any individual client.
Dr Rosemary Listing, PhD (Law), Medical negligence lawyer since 2014 · Of Counsel, Peter Evans & Associates. Rosemary's doctorate examined patterns of failure in medical negligence, and she teaches health law at the University of Newcastle. She is not medically qualified. About Rosemary.
Last updated: 10 November 2026 · First published: 10 November 2026 · Next review: May 2027
Cite this article: Listing R. “I could see metal through my skin”: When a stimulator battery breaks through. Reframe Legal. Published 10 November 2026. https://reframelegal.com/stimulator-breaking-through-skin/
This article is general information, not legal or medical advice. It does not create a lawyer–client relationship. Speak to your treating clinicians about your health, and get legal advice about your own situation.
If you are in danger or need urgent medical help, call 000. For crisis support, call Lifeline on 13 11 14.
Legal services are provided by Peter Evans & Associates.