The shock device has still not been FDA tested even though the FDA was instructed to do so in 2011 and, if you review the history and the law, should have happened decades ago.
This safety down-classification must not take place!
The FDA, shock machine manufacturers and Psychiatric organization must be be held accountable. Requiring Accountability, transparency and unbiased testing, damage acknowledgement and support for those injured and true informed consent is not an unreasonable request! #FDAStoptheShockDevicehttps://www.change.org/p/fda-stop-fda-from-down-classifying-the-shock-device-to-a-class-ii-device-stop-shock-treatment