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Common allegations in spinal cord stimulator lawsuits include: Defective design or manufacturing that caused a device to malfunction Lead migration, lead fracture, battery failure, or loss of effective stimulation Painful electrical shocks, burning sensations, neurological injury, or autonomic dysfunction Inadequate testing of devices or significant post-approval modifications Failure to warn patients and physicians about known risks and the potential need for revision surgery or device removal Failure to submit required safety information or adverse event reports to the FDA Misrepresentations about device safety, effectiveness, or expected pain relief Improper involvement by manufacturer representatives in device placement, programming, or treatment decisions What is the Average Spinal Stimulator Lawsuit Settlement Amount