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Calls for COVID-19 vaccine recall – FDA’s own study finds DNA contamination in Pfizer vaccines

Published

6 months ago

8 minute read

From LifeSiteNews

By Dr. Michael Nevradakis for The Defender

“It is alarming that the public is made aware of this contamination in an obscure journal that features high school science research. One has to ask, ‘Where is the FDA now?’ and ‘Why hasn’t the public been alerted of this?’”

The peer-reviewed study in the Journal of High School Science was authored by three high school students and performed at an FDA lab under the supervision of FDA scientists. The findings prompted renewed calls for a moratorium on COVID-19 vaccines.

A peer-reviewed study performed at a U.S. Food and Drug Administration (FDA) laboratory by high school students has confirmed the presence of a high level of DNA contamination in Pfizer’s mRNA COVID-19 vaccine.

The study, published December 29, 2024, in the Journal of High School Science, was authored by three students at Centreville High School in Clifton, Virginia, and performed under the supervision of FDA scientists.

Maryanne Demasi, Ph.D., an investigative medical reporter, was the first to report on the study.

READ: British doctor has medical license revoked over warning of COVID shot dangers

The research, performed at the FDA’s White Oak Campus in Maryland, found that levels of residual DNA in the Pfizer COVID-19 vaccine were 6 to 470 times higher than regulatory safety limits. The students tested two lots of the vaccine, finding they contained “residual DNA to a level that exceeds 10 ng [nanograms] per dose.”

“The potential health risk posed by residual small DNA fragments is currently unknown,” the study stated. However, the authors also said that DNA contamination may result in insertional mutagenesis –  or DNA mutations – that can cause cancer.

Speaking last month on “The Defender In-Depth,” Kevin McKernan, who first identified DNA contamination in the shots in 2023, said DNA in vaccines can pose health risks because the DNA “could integrate into the genome and cause disruption of the genome … or it could disrupt other genes that are related to cancer.”

The FDA did not respond to multiple requests for comment on the study.

COVID vaccines ‘must be immediately recalled’

The new findings challenge “years of dismissals by regulatory authorities, who had previously labelled concerns about excessive DNA contamination as baseless,” Demasi wrote on Substack.

The findings also align with earlier reports from independent laboratories in the U.S., Canada, Australia, Germany, and France, she said.

McKernan, founder of Medicinal Genomics, told The Defender that eight studies have found DNA over the limit. “Very few studies are surveying a large number of lots, so each study is additive,” he said.

Epidemiologist Nicolas Hulscher said that in “light of this evidence, the COVID-19 genetic injections must be immediately recalled, to protect the public from further harm.”

Nikolai Petrovsky, Ph.D., director of biotechnology company Vaxine Pty Ltd., told Demasi that the findings are a “smoking gun” and that the new study “clearly shows the FDA was aware of these data.”

Christof Plothe, D.O., a member of the World Council for Health steering committee, agreed. He said:

So far, the European, Australian, and American health regulatory boards have denied any risks from plasmid DNA contamination in the COVID-19 injections despite nine studies by internationally known research teams.

All teams concluded that this contamination poses an unacceptable risk to three-quarters of the world’s population.… Three teams so far have demonstrated the integration into human cells. To what extent this is happening to everybody who was injected needs to be investigated.

McKernan said that the FDA has long ignored evidence of the dangers posed by mRNA COVID-19 vaccines.

“The criteria for pulling these shots was established long before DNA contamination was first discovered,” he said. “I would hope that evidence of highly variable manufacturing would be grounds for immediate class 1 recall from the FDA. They are currently distracted with performing class 1 recalls on non-lethal hairspray.”

A Class 1 recall involves “a situation in which there is a reasonable probability that the use of, or exposure to, a violative product will cause serious adverse health consequences or death.”

According to Demasi, “The FDA is expected to comment on the findings this week. However, the agency has yet to issue a public alert, recall the affected batches, or explain how vials exceeding safety standards were allowed to reach the market.”

Plothe noted that Demasi presented evidence of DNA contamination to the FDA in September 2024, asking if the agency had launched an investigation or requested further testing of the mRNA vaccines by their manufacturers.

“Nothing resulted from this request,” Plothe said. “As nine studies have proven this severe contamination and repeated requests to health regulatory boards have not led to any consequence, we must ask about the motive.”

Brian Hooker, Ph.D., chief scientific officer for Children’s Health Defense (CHD), noted the irony of high school students discovering what the FDA has seemingly missed in the four-plus years since the vaccines’ introduction.

“It is ironic that it takes student researchers at the FDA to do the work of the FDA regulators,” Hooker said. “It is alarming that the public is made aware of this contamination in an obscure journal that features high school science research. One has to ask, ‘Where is the FDA now?’ and ‘Why hasn’t the public been alerted of this?’”

Demasi said that the significance of the new study’s findings is that they came from research performed at an FDA facility.

“Now that DNA contamination of the mRNA vaccines has been verified in the laboratory of an official agency and published in a peer-reviewed journal, it becomes difficult to ignore,” Demasi wrote. “It also places vaccine manufacturers and regulators in a precarious position.”

This article was originally published by The Defender – Children’s Health Defense’s News & Views Website under Creative Commons license CC BY-NC-ND 4.0. Please consider subscribing to The Defender or donating to Children’s Health Defense.

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Published on July 14, 2025

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From LifeSiteNews

By Clare Marie Merkowsky

Carney’s Liberal government signed nearly $400 million in contracts with Pfizer and Moderna for COVID shots, despite halted booster programs and ongoing delays in compensating Canadians for jab injuries.

Prime Minister Mark Carney has awarded Pfizer and Moderna nearly $400 million in new COVID shot contracts.

On June 30th, the Liberal government quietly signed nearly $400 million contracts with vaccine companies Pfizer and Moderna for COVID jabs, despite thousands of Canadians waiting to receive compensation for COVID shot injuries.

The contracts, published on the Government of Canada website, run from June 30, 2025, until March 31, 2026. Under the contracts, taxpayers must pay $199,907,418.00 to both companies for their COVID shots.

Notably, there have been no press releases regarding the contracts on the Government of Canada website nor from Carney’s official office.

Additionally, the contracts were signed after most Canadians provinces halted their COVID booster shot programs. At the same time, many Canadians are still waiting to receive compensation from COVID shot injuries.

Canada’s Vaccine Injury Support Program (VISP) was launched in December 2020 after the Canadian government gave vaccine makers a shield from liability regarding COVID-19 jab-related injuries.

There has been a total of 3,317 claims received, of which only 234 have received payments. In December, the Canadian Department of Health warned that COVID shot injury payouts will exceed the $75 million budget.

The December memo is the last public update that Canadians have received regarding the cost of the program. However, private investigations have revealed that much of the funding is going in the pockets of administrators, not injured Canadians.

A July report by Global News discovered that Oxaro Inc., the consulting company overseeing the VISP, has received $50.6 million. Of that fund, $33.7 million has been spent on administrative costs, compared to only $16.9 million going to vaccine injured Canadians.

The PHAC’s downplaying of jab injuries is of little surprise to Canadians, as a 2023 secret memo revealed that the federal government purposefully hid adverse effect so as not to alarm Canadians.

The secret memo from former Prime Minister Justin Trudeau’s Privy Council Office noted that COVID jab injuries and even deaths “have the potential to shake public confidence.”

“Adverse effects following immunization, news reports and the government’s response to them have the potential to shake public confidence in the COVID-19 vaccination rollout,” read a part of the memo titled “Testing Behaviourally Informed Messaging in Response to Severe Adverse Events Following Immunization.”

Instead of alerting the public, the secret memo suggested developing “winning communication strategies” to ensure the public did not lose confidence in the experimental injections.

Since the start of the COVID crisis, official data shows that the virus has been listed as the cause of death for less than 20 children in Canada under age 15. This is out of six million children in the age group.

The COVID jabs approved in Canada have also been associated with severe side effects, such as blood clots, rashes, miscarriages, and even heart attacks in young, healthy men.

Additionally, a recent study done by researchers with Canada-based Correlation Research in the Public Interest showed that 17 countries have found a “definite causal link” between peaks in all-cause mortality and the fast rollouts of the COVID shots, as well as boosters.

Interestingly, while the Department of Health has spent $16 million on injury payouts, the Liberal government spent $54 million COVID propaganda promoting the shot to young Canadians.

The Public Health Agency of Canada especially targeted young Canadians ages 18-24 because they “may play down the seriousness of the situation.”

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FDA requires new warning on mRNA COVID shots due to heart damage in young men

Published on July 12, 2025

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From LifeSiteNews

By Doug Mainwaring

Pfizer and Moderna’s mRNA COVID shots must now include warnings that they cause ‘extremely high risk’ of heart inflammation and irreversible damage in males up to age 24.

The Trump administration’s Food and Drug Administration (FDA) announced it will now require updated safety warnings on mRNA COVID-19 shots to include the “extremely high risk” of myocarditis/pericarditis and the likelihood of  long-term, irreversible heart damage for teen boys and young men up to age 24.

The required safety updates apply to Comirnaty, the mRNA COVID shot manufactured by Pfizer Inc., and Spikevax, the mRNA COVID shot manufactured ModernaTX, Inc.

According to a press release, the FDA now requires each of those manufacturers to update the warning about the risks of myocarditis and pericarditis to include information about:

  1. the estimated unadjusted incidence of myocarditis and/or pericarditis following administration of the 2023-2024 Formula of mRNA COVID-19 shots and
  2. the results of a study that collected information on cardiac magnetic resonance imaging (cardiac MRI) in people who developed myocarditis after receiving an mRNA COVID-19 injection.

The FDA has also required the manufacturers to describe the new safety information in the adverse reactions section of the prescribing information and in the information for recipients and caregivers.

Additionally, the fact sheets for healthcare providers and for recipients and caregivers for Moderna COVID-19 shot and Pfizer-BioNTech COVID-19 shot, which are authorized for emergency use in individuals 6 months through 11 years of age, have also been updated to include the new safety information in alignment with the Comirnaty and Spikevax prescribing information and information for recipients and caregivers.

In a video published on social media, Dr. Vinay Prasad, director of the Center for Biologics Evaluation & Research Chief Medical and Scientific Officer, explained the alarming reasons for the warning updates.

While heart problems arose in approximately 8 out of 1 million persons ages 6 months to 64 years following reception of the cited shots, that number more than triples to 27 per million for males ages 12 to 24.

Prasad noted that multiple studies have arrived at similar findings.

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