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Can You Finally Sue Pharmaceutical Manufacturers For COVID-19 Shot? DNA Contamination Disclosed?

According to entrepreneur and Vaccine Safety Research Foundation founder Steve Kirsch, you can now sue mRNA COVID-19 jab manufacturers for damages.

“You can now sue the mRNA COVID vaccine manufacturers for damages and the FDA is required to take the COVID vaccines off the market. Why? Adulteration,” Kirsch said.

“The plasmid bioactive contaminant sequences were NOT pointed out to the regulatory authorities. It’s considered adulteration. I just got off the phone with Professor Byram Bridle and Dr. Robert Malone on this,” he added.

“Michigan remdesivir case is very important precedent here proving liability shield falls when there is undisclosed contamination of active ingredients,” he said.

“The FDA is now at a crossroads. 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,” Kirsch explained.

“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,” he added.

“The SV40 promoter is found in all the vials and it was in the gene sequence that was provided to the regulators. There is no mistake. The problem was that neither drug company ever pointed it out to the regulators. It’s an unapproved contaminant that doesn’t meet the standards set,” Kirsch said.

“So the regulators are off the hook. But if the regulators don’t take action, then they dig themselves into a very deep hole. The law requires the FDA to stop the vaccine,” he continued.

“Dr. Naomi Wolf reports that SV40 does not appear in any of the regulatory documents that Pfizer gave the FDA. So it’s an active ingredient that was not disclosed. That makes it adulteration. This means that the FDA is required to take it off the market. NOW,” Kirsch wrote.

“A writ of mandamus can be used to force the FDA to follow the law. Also, a court injunction could halt both mRNA vaccines in the US immediately. But this would require a showing of ‘irreparable harm’ (among other criteria). If we can prove that the plasmid contamination is causing “irreparable harm” (i.e., integrating into your DNA), the vaccine is TOAST,” Kirsch explained.

“So can you guess what we are working on now? Isn’t it stunning that the FDA hasn’t even issued a Warning Letter to either manufacturer? That neither manufacturer has taken any voluntary actions to investigate this? That the FDA and CDC haven’t even alerted the public that there might be a MAJOR problem here?” he added.

In a preprint paper titled “DNA fragments detected in monovalent and bivalent Pfizer/BioNTech and Moderna modRNA COVID-19 vaccines from Ontario, Canada: Exploratory dose response relationship with serious adverse events,” the researchers write:

In vitro transcription (IVT) reactions used to generate nucleoside modified RNA (modRNA) for SARS-CoV-2 vaccines currently rely on an RNA polymerase transcribing from a DNA template. Production of modRNA used in the original Pfizer randomized clinical trial (RCT) utilized a PCR-generated DNA template (Process 1). To generate billions of vaccine doses, this DNA was cloned into a bacterial plasmid vector for amplification in Escherichia coli before linearization (Process 2), expanding the size and complexity of potential residual DNA and introducing sequences not present in the Process 1 template. It appears that Moderna used a similar plasmid-based process for both clinical trial and post-trial use vaccines. Recently, DNA sequencing studies have revealed this plasmid DNA at significant levels in both Pfizer-BioNTech and Moderna modRNA vaccines. These studies surveyed a limited number of lots and questions remain regarding the variance in residual DNA observed internationally.

Methods: Using previously published primer and probe sequences, quantitative polymerase chain reaction (qPCR) and Qubit® fluorometry was performed on an additional 27 mRNA vials obtained in Canada and drawn from 12 unique lots (5 lots of Moderna child/adult monovalent, 1 lot of Moderna adult bivalent BA.4/5, 1 lot of Moderna child/adult bivalent BA.1, 1 lot of Moderna XBB.1.5 monovalent, 3 lots of Pfizer adult monovalent, and 1 lot of Pfizer adult bivalent BA.4/5). The Vaccine Adverse Events Reporting System (VAERS) database was queried for the number and categorization of adverse events (AEs) reported for each of the lots tested. The content of one previously studied vial of Pfizer COVID-19 vaccine was examined by Oxford Nanopore sequencing to determine the size distribution of DNA fragments. This sample was also used to determine if the residual DNA is packaged in the lipid nanoparticles (LNPs) and thus resistant to DNaseI or if the DNA resides outside of the LNP and is DNaseI labile.

“Kevin McKernan is a friend of mine and his work is unimpeachable. His results have been replicated by others all over the world. He found that the COVID vaccines contain therapeutic levels of plasmid DNA. DNA lasts forever, and if it integrates into your genome, you will produce its product forever,” Steve Kirsch writes.

From Steve Kirsch’s Newsletter:

The main takeaways are:

  1. The mRNA vaccines are contaminated with SV40 and who knows what else. This should never have been allowed.
  2. The vials exceeded the guidelines by “orders of magnitude.”
  3. The discovery was confirmed by Health Canada.
  4. The FDA and CDC are remaining silent. As far as anyone knows, they are no doing anything to assess the implications of the finding. I presume that they must believe that by not knowing the implications, they won’t have to disclose them so they are better protecting themselves against the public who might be very upset to learn they were guinea pigs. But that’s just an educated guess.
  5. We don’t know what the implications are. Experts disagree. Some claim the contamination is meaningless. Others say it could be very serious.
  6. The experts who claim there is no risk of harm have NO EVIDENCE to back up their claims. So that’s really comforting, isn’t it? Trust the experts :). Don’t worry.
  7. The politicians seem happy to let YOU take the risk. And they aren’t giving you any informed consent about this issue. Nobody seems to be requesting the CDC warn anyone of the potential risk. Wouldn’t want to scare anyone, would we?
  8. It was not the government regulators who first discovered the contamination. It was my friend Kevin McKernan. This should never have happened. The government should have discovered this at the very outset, 3 years ago.
  9. It would have been discovered sooner by independent researchers, but people were threatened with arrest if they supplied vials for analysis. I know this first hand because I was warned I would be arrested and criminally charged if I participated in trying to analyze the vials.
  10. We don’t fully know the ramifications of the contamination, but they probably aren’t good, and they could be devastating and irreversible. We don’t know yet because nobody has done the necessary studies.
  11. The experts I consulted thought that it was likely to be very serious. But they couldn’t quantify “likely” but said only that it was “more likely than not.”
  12. I volunteered for a full gene sequencing study, but they said they’d have to cut off my deltoid muscle, so I changed my mind.
  13. The regulators apparently never QAed any of the vials. If they did, they would have found contaminations such as this before it was ever injected into a single human being. Or they did and simply chose to remain silent and look the other way. Health Canada said the sequence was disclosed to them, but that the drug company never pointed out that the SV40 promoter sequence was specifically identified in the gene sequence provided.
  14. The SV40 promoter contamination has been known since April 9, 2023 when McKernan published a paper on it. But the CDC and FDA have remained silent on this issue. That’s comforting, isn’t it? <sarcasm off>
  15. The mainstream media is silent as well.
  16. And the mainstream medical community is silent as well. After all, they recommended you injected the stuff so they are not going to admit they fucked up, are they?
  17. There is absolutely no doubt this is happening, so the silence of the formerly “trusted” health authorities is telling.
  18. The longer they delay telling you they forgot to QA the vials, the bigger the hole they are going to dig for themselves.

According to The Epoch Times Canada contributor Noé Chartier, “Health Canada Confirms Undisclosed Presence of DNA Sequence in Pfizer Shot.”

“Simian Virus 40 enhancer was not disclosed by Pfizer, but Health Canada located it after Kevin McKernan and PJ Buckhaults made their findings of DNA contamination public,” he said.

“In what one scientist described as an ‘admission of epic proportions,’ Health Canada on Thursday confirmed the presence of DNA contamination in Pfizer COVID-19 vaccines, and also confirmed that Pfizer did not disclose the contamination to the public health authority,” The Defender writes.

Per The Defender:

The DNA contamination includes the Simian Virus 40 (SV40) promoter and enhancer Pfizer did not previously disclose and that some experts say is a cancer risk due to potential integration with the human genome.

Health Canada, the country’s public health authority, told The Epoch Times that while Pfizer provided the full DNA sequences of the plasmid in its vaccine at the time of the initial submission, the vaccine maker “did not specifically identify the SV40 sequence.”

“Health Canada expects sponsors to identify any biologically functional DNA sequences within a plasmid (such as an SV40 enhancer) at the time of submission,” it said.

Health Canada’s admission came after two scientists, Kevin McKernan and Phillip J. Buckhaults, Ph.D., discovered the presence of bacterial plasmid DNA in the mRNA COVID-19 vaccines at levels potentially 18-70 times higher than the limits set by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency.

They tested four expired Pfizer and Moderna vaccine vials “thought to only contain mRNA” and found to contain “double-stranded DNA plasmids.”

Health Canada said, “We have concluded that the risk/benefit profile continues to support the use of the Pfizer-BioNTech vaccine,” and that it does rely on manufacturer claims but “conducts an in-depth independent review” to make sure the vaccines meet “our high standards for safety, efficacy and quality.”

Janci Lindsay, Ph.D., director of toxicology and molecular biology for Toxicology Support Services, told The Defender this statement is “silly, not believable and not defendable,” adding that “We should not have to do the research that they should have done.”

“Why are the FDA, CDC [Centers for Disease Control and Prevention] and the mainstream media still silent about this?” asked Steve Kirsch, founder of the Vaccine Safety Research Foundation, adding that “the mainstream medical community is silent as well.”

Viral immunologist Dr. Byram Bridle of the University of Guelph in Canada, commenting on Health Canada’s admission wrote on his Substack, “This is an admission of epic proportions.”

The Canadian Independent writes:

Must Watch: Dr. Byram Bridle unveils recent discoveries of DNA contamination present in the Pfizer and Moderna COVID-19 vaccines. He suggests that this revelation could serve as compelling evidence to pursue legal action against the manufacturers.

Dr. Byram Bridle joined the World Council for Health to explain new findings of DNA contamination in the Pfizer and Moderna COVID-19 vaccines. While some of Dr. Byram’s explanations about the contamination may pose a challenge for the average person to understand, the essence of his message is clear: the Pfizer and Moderna COVID-19 vaccines are contaminated.

Towards the end of the video, starting at the 15:39:30 mark, Dr. Bridle explains how attorneys could leverage this discovery to pursue legal action against manufacturers. Importantly, Dr. Byram highlights that this DNA contaminant was not disclosed by the manufacturers during the authorization process.

WATCH:

Watch the entire World Council for Health meeting via Rumble:


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