by Michael Nevradakis, Ph.D. at the Defender
Scientists and legal experts have petitioned the U.S. Food and Drug Administration (FDA) to suspend or withdraw the Pfizer and Moderna mRNA COVID-19 vaccines, arguing they are unapproved gene therapies and citing their contamination with DNA plasmids.
According to a press release by Australian law firm PJ O’Brien & Associates, the petition “exposes alarming evidence of synthetic DNA contamination and regulatory failures that could affect millions worldwide,” shedding light on “a public health crisis.”
The Citizen Petition stated that Pfizer and Moderna misclassified their mRNA products as vaccines instead of gene therapy products, enabling the companies to avoid legally required FDA environmental assessments.
“This misclassification denied Americans transparency and informed consent, violating federal law and rendering approvals void from the start,” the press release stated.
The petition also cites several studies that “confirm synthetic DNA in these vaccines at levels 6 to 470 times above safety thresholds.”
“This biologically active DNA — detected in vials and human blood — carries SV40 [simian virus 40] sequences linked to cancer and genomic instability, posing risks of oncogenesis, hereditary changes, and immune disruption,” the press release stated.
The petition calls on the FDA to investigate its classification of the mRNA shots as non-gene therapy products,…
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