
FIND OUT IF YOUR CASE QUALIFIES
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Spinal Cord Stimulator — Free Case Review
Abbott or St. Jude stimulator problems?
A JPML decision on Abbott consolidation is expected this fall. See if your case qualifies now.
ACTIVE LITIGATION — NO SETTLEMENT. MDL 3181 underway · deadlines vary by state.
Do you — or someone you love — have a spinal cord stimulator that caused problems?
Check if my case qualifiesfree · takes 2 minutes
I’m not sure it was the device →
No documents needed · an answer either way · no fee unless there is a recovery. Court costs and litigation expenses are advanced by counsel and repaid from the recovery. You are not responsible for court costs or litigation expenses if there is no recovery, unless a court directs otherwise. The attorney’s fee is a percentage of the gross recovery, calculated before expenses are deducted.
Or talk to a person now: (888) 348-2735 — answered 24/7
Stefanie A. Murphy & Matthew T. Marin
Partners
Every spinal cord stimulator inquiry gets a personal review — and an honest answer either way, free and without obligation.
Claims target the device manufacturers — not your doctor. Some matters may be referred to other lawyers. No settlement has been reached, and most cases are in their earliest stages; every case must be proven on its own facts. Attorney Advertising.
Abbott Laboratories — which acquired St. Jude Medical’s stimulator business — faces mounting lawsuits over its Proclaim, Infinity, and Eterna spinal cord stimulators, and it is the only SCS manufacturer whose devices are subject to a Class I recall, the FDA’s most serious category. On June 29, 2026, plaintiffs petitioned the JPML to consolidate the federal Abbott cases; a decision is expected this fall. This page updates the day the Panel rules.
Free Confidential Evaluation — No Fee Unless There Is a Recovery Court costs and litigation expenses are advanced by counsel and repaid from the recovery. You are not responsible for court costs or litigation expenses if there is no recovery, unless a court directs otherwise. The attorney’s fee is a percentage of the gross recovery, calculated before expenses are deducted.
Call (888) 348-2735 — available 24/7, a person answers.
See if you qualify
A few quick questions about your spinal cord stimulator, the problems you experienced, and any revision or removal surgery. This is the initial intake screening, not a full case review. Most people finish in about two minutes.
- 🔒 Confidential
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- ⏱ ~2 minutes
Marin & Murphy Law Firm · Free & confidential · Stop messages anytime
Marin & Murphy Law Firm is currently accepting spinal cord stimulator cases. Free, confidential case reviews: (888) 348-2735, available 24/7.
The 2023 Class I recall — check your device
Abbott recalled approximately 198,000 Proclaim and Infinity devices (~155,000 in the U.S.) because they could become stuck in MRI mode, leaving patients without stimulation — and unable to restore it — after an MRI. If you received a recall letter, keep it. Don’t know if your device is affected? Your patient ID card or charger identifies your model in under two minutes — and if not, your operative report names it and we obtain it for you.
Litigation updates
June 29, 2026: JPML centralization petition filed for the federal Abbott cases (decision expected fall 2026). June 5, 2026: the Panel declined to fold four pending Abbott cases into the Boston Scientific MDL, leaving the Abbott track to develop separately. A new individual Abbott case was filed in the District of South Carolina on July 31, 2026.
What plaintiffs allege
Sales representatives programming devices without physician supervision — effectively practicing medicine without a license · rapid lead migration and electrical shocks · devices trapped in MRI mode (the recall defect) · battery and charging failures including heat at the implant site · hundreds of post-approval modifications with minimal new clinical testing — FDA records show 241 supplements on the legacy St.
Jude system (P010032) and 92 on the DRG system (P150004), with only a handful of panel-track clinical reviews. Since 2020, FDA’s MAUDE database contains roughly 84,000 adverse event reports naming Abbott/St. Jude neurostimulation devices — the most of any SCS manufacturer (reports are not verified causation).
Devices involved
- Proclaim™ XR
- Proclaim™ Plus
- Proclaim™ DRG
- Infinity™ 5/7
- Eterna™
- legacy St. Jude Eon™/Eon Mini™
Do you qualify?
You may qualify if you received one of these devices and experienced any of the following:
- ✓ Revision, replacement, or removal (explant) surgery
- ✓ Electrical shocks, jolts, or burning at the battery site
- ✓ Lead migration or fracture shown on imaging
- ✓ Infection requiring treatment or surgery
- ✓ New weakness, numbness, paralysis, or bowel/bladder problems
“It just stopped working”? Alone, generally not enough — paired with any additional procedure, it is. Many people disqualify themselves wrongly; the review is free.
Free Confidential Evaluation — No Fee Unless There Is a Recovery
Call (888) 348-2735 — available 24/7, a person answers.
Matthew T. Marin, J.D. — Admitted in Rhode Island, South Carolina, Connecticut, and Massachusetts
Stefanie A. Murphy, J.D. — Admitted in Rhode Island, Connecticut, and Massachusetts
Frequently Asked Questions
Sources (5)
- FDA Recall database, Abbott Proclaim/Infinity Class I recall (2023).
- FDA PMA database, P010032 and P150004 supplement records.
- FDA MAUDE database, product code LGW (reports are not verified causation).
- JPML docket, petition for centralization of Abbott SCS actions (filed June 29, 2026).
- U.S. District Court, D.S.C., Dkt. 4:26-cv-03174 (filed July 31, 2026).
Read next
Attorney Advertising. This page is general information, not legal advice, and does not create an attorney-client relationship — that relationship is formed only by a signed written agreement. The attorneys of Marin & Murphy Law Firm are licensed in Rhode Island, South Carolina, Connecticut, and Massachusetts. We evaluate potential claims nationwide; for matters arising in states where our attorneys are not admitted, we associate with or refer to locally licensed co-counsel and do not ourselves practice law in those jurisdictions. Submitting the contact form or contacting the firm does not create an attorney-client relationship. Representation is offered on a contingent-fee basis: no fee unless there is a recovery, though a client may be responsible for case costs and expenses. The statute of limitations may sharply limit the time to file a claim. Prior results do not guarantee a similar outcome, and no outcome is guaranteed. Responsible attorney: Matthew T. Marin, Marin & Murphy Law Firm (South Carolina).