If you were implanted with a Nevro HF10 spinal cord stimulator and later experienced serious complications, you may qualify for compensation.
Nevro's HF10 spinal cord stimulator is an implanted device marketed to manage chronic pain by delivering electrical pulses along the spine. Lawsuits filed against Nevro allege the device is defectively designed and was improperly programmed by sales representatives who lacked adequate medical training, and that the company overstated its safety and effectiveness in marketing materials.
Plaintiffs allege the device can overstimulate the vagus nerve — which helps regulate heart rhythm, digestion, and other involuntary body functions — leading to complications such as irregular heartbeat, bowel dysfunction, and incontinence. Cases are currently proceeding individually in federal court while plaintiffs seek to have them formally consolidated for coordinated pretrial handling.
Here's what happens after you reach out:
A short set of free eligibility questions about your situation — takes about two minutes.
Our network reviews your answers against current qualifying criteria and reaches out if you may qualify.
You decide whether to move forward. There's never a cost to check your eligibility.
Multiple Nevro spinal cord stimulator lawsuits have been filed in federal court, including a group of cases brought simultaneously in the Northern District of California, and plaintiffs' attorneys have asked the federal judicial panel to formally consolidate the growing number of cases. The litigation is still in its early stages, with lawyers continuing to investigate and file new claims. Because early litigation can move quickly once a device gets more attention, a free eligibility review is the fastest way to find out what may apply to your situation.
A federal panel will hear arguments September 24, 2026 on whether to centralize Nevro spinal cord stimulator injury lawsuits into a new MDL, over the manufacturer's objection that the cases lack common defect and injury allegations.
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