Janelle Schnulle, Plantiff v, Somatics LLC, Defendant, case number 4:21-CV-00109 JCH
According to public record, Janelle Schnulle had 33 electroconvulsive therapy (ECT) treatments from April 2015 through January 2016 at Mercy Hospital, St. Louis.
She claims the ECT treatments caused permanent neurological damage that impaired her ability to learn and retain information.
In her lawsuit against ECT device manufacturer, Somatics LLC, Schnulle alleges the company was aware of serious risks but did nothing to warn the public or doctors they failed to properly research and test the ECT device, investigate bad outcomes or report adverse events with the FDA, provide sufficient warnings to medical community and the public, investigate or properly report adverse events to the FDA or comply with federal law.
Read more a in-depth lawsuit summary – VitalLaw
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Further Reading & Action
History of the FDA’s regulation of the ECT device – The FDA’s Regulation of ECT (Shock Treatment): A Beginner (or Refresher) Course | NARPA
Somatics LLC previous lawsuit – ECT Lawsuit Victory – Riera v. Somatics, LLC, 2018
Somatics LLC admits device causes brain damage in regulatory update – ECT Device Manufacturer Acknowledges Brain Damage as a Risk of Electroconvulsive Therapy
The impact of litigation – ECT Device Maker Mecta Corp. Files Chapter 11 After Lawsuits Hinder Access to Liability Insurance
How to file a ECT lawsuit – Litigation tips
How to file an adverse medical harm report – Action page