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How to Report Your ECT Injuries to the FDA
“Plaintiff alleges that undergoing ECT treatment with this device caused permanent neurological damage impairing his ability to memorize, retain, and recall information. Plaintiff further alleges that despite knowing of the substantial risks associated with ECT treatment, Somatics and Elektrika manufactured and distributed the device and failed to warn Plaintiff of those risks.”
Janelle Schnulle had 33 ECT treatments she claims caused permanent neurological damage. She is suing device manufacturer, Somatics LLC.
The use of electroshock is a consistent concern of MHEP, particularly when it is forced, court-ordered, or delivered without informed consent of its many risks, on children and adults.
Testimony Prepared for the Standing Committee on Mental Health of the Assembly of the State of New York.
October 5, 1978. by Dr. Peter Sterling, Ph.D. Associate Professor of Neurobiology.
On September 30, 2021, ECT device manufacturer Mecta Corp. filed chapter 11 bankruptcy amid lawsuits hindering their liability insurance eligibility.
Financial pressure from combined lawsuits and lack of insurance led to the discontinuation of the SpECTrum device On September 1st, 2021, according to the Debtors.
I am a survivor of ECT. I had a fairly typical experience. Five years of my life were permanently erased as if they had never happened, including most of my college education; I lost 40 points off my IQ; and I’ve been left with permanent disabling memory and cognitive deficits.
ECT Device Manufacturer Somatics, LLC, acknowledged lasting damage caused by electroconvulsive therapy in a regulatory update following the groundbreaking 2018 lawsuit, Riera v. Somatics, LLC.