Contrary to popular belief, it is actually now possible to sue the pharmaceutical companies responsible for these adulterated injections, the mRNA varieties of which were found to contain plasmid bioactive contaminant sequences that were never revealed to regulatory authorities prior to their emergency use authorization (EUA) and later approval.
The U.S. Food and Drug Administration (FDA) was never told by Pfizer-BioNTech or Moderna that their respective messenger RNA shots are contaminated with these foreign, toxic substances. As such, anyone can now sue these vaccine manufacturers – and according to the law, the FDA must respond by pulling these deadly drugs off the market.
According to Kirsch, the Michigan remdesivir case sets an important precedent for all this in that it has shown that the liability shield afforded by Big Pharma disintegrates the moment any undisclosed contamination of the jabs' active ingredients is proven.
"The FDA is now at a crossroads," Kirsch says. "Either they admit that they knew about the plasma contamination, and failed to disclose that to the public and to the outside committees, or they can claim that they didn't know about it in which case Pfizer is liable."
"But we have the Pfizer documents that were given to the FDA so we know what the FDA got. And I seriously doubt there's any disclosure of SV40 contamination. That means we have an adulterated vaccine and the FDA has to remove it from the market until the adulteration is fixed. If the FDA doesn't do that, they should face criminal prosecution for endangering the public, and not following the law."...<<<Read More>>>...
