• Petition filed by scientists and legal experts calls for immediate suspension of Pfizer and Moderna mRNA COVID-19 vaccines

• Evidence reveals synthetic DNA contamination up to 470 times above safety limits, including cancer-linked SV40 sequences

• FDA accused of unlawfully classifying mRNA shots as vaccines instead of gene therapies, bypassing critical safety reviews

• Experts warn of genomic instability, immune disorders, and cancer risks from contaminated injections

A global reckoning: FDA complicity in a public health disaster

In a damning indictment of the U.S. Food and Drug Administration (FDA), a coalition of scientists, immunologists, and legal experts has filed a formal petition demanding the immediate suspension or withdrawal of Pfizer and Moderna’s mRNA COVID-19 vaccines. The petition, now open for public comment, exposes shocking evidence of synthetic DNA contamination, regulatory fraud, and the deliberate misclassification of these experimental gene therapies as “vaccines”—a deception that has placed millions at risk of irreversible harm.

The petition, spearheaded by Australian law firm PJ O’Brien & Associates, accuses the FDA of enabling one of the greatest medical frauds in modern history. By greenlighting Pfizer and Moderna’s mRNA injections without proper environmental assessments—a legal requirement for gene therapies—the agency allowed these dangerous products to flood the market under the false pretense of “emergency use.”

“This misclassification denied Americans transparency and informed consent, violating federal law and rendering approvals void from the start,” the petition states.

Among the petition’s signatories are prominent figures such as attorney Julian J. Gillespie, immunologist Dr. Jessica Rose, and virologist Dr. David J. Speicher. Kevin McKernan, chief scientific officer of Medicinal Genomics and the first to uncover DNA contamination in the shots, warns that the FDA’s silence is indefensible.

“How do they ever expect to regain the public’s trust?” McKernan asked. “They recently recalled some protein bars for a threat of peanut allergies, yet every American knows multiple people with COVID-19 vaccine injuries, yet the FDA is head-in-the-sand silent.”

DNA contamination: a ticking time bomb in every dose

Independent studies cited in the petition reveal that Pfizer and Moderna’s mRNA injections contain synthetic DNA at levels 6 to 470 times above safety thresholds, including SV40 promoter sequences—a known cancer risk. These contaminants, shielded by lipid nanoparticles (LNPs), can integrate into human DNA, triggering genomic instability, immune dysfunction, and malignancies.

• A September 2023 study by McKernan found DNA contamination 18 to 70 times above regulatory limits.

• An FDA-supervised study in December 2024 confirmed contamination up to 470 times over safety limits.

• German and French researchers have replicated these findings, proving this is not an isolated issue but a systemic failure.

“This is not just an American crisis—it’s a global reckoning,” Gillespie declared. “Governments must act now to halt further harm and support those already affected.”

FDA’s unlawful approval: rewriting the rules to protect Big Pharma

The petition exposes how Pfizer and Moderna exploited regulatory loopholes by falsely labeling their mRNA products as “vaccines” instead of gene therapies. Under U.S. law, gene therapies require rigorous environmental assessments—a step the FDA illegally bypassed.

“Had the FDA properly demanded Environmental Assessments, the American public would have been informed of the gene therapy nature of these shots,” the petition states. Instead, the agency colluded with manufacturers to fast-track untested, hazardous technology into the arms of billions.

Dr. Jessica Rose minced no words: “The petition evidences potent facts that should lead to the suspension of use of these experimental nucleoside-modified RNA gene-based products.”

As the petition lands on the desk of HHS Secretary Robert F. Kennedy Jr., the world watches to see if the U.S. government will finally hold the FDA and Big Pharma accountable? With mounting evidence of genetic contamination, regulatory fraud, and catastrophic health consequences, one question remains: How many more lives must be destroyed before the FDA admits its crimes?

Ending a reckless genetic experiment that should have never been approved in the first place

The so-called “COVID vaccines” were never vaccines—they were unproven, reckless genetic experiments forced upon the public under the guise of emergency use. These mRNA-based injections, fraudulently marketed as life-saving, were in fact biological weapons that corrupted human cellular machinery, forcing cells to produce a foreign, toxic spike protein with devastating consequences.

From the outset, these injections should have never been authorized, let alone mandated. Clinical trials were rushed, safety signals ignored, and adverse effects brushed aside as “rare” while thousands suffered heart damage, neurological disorders, and immune dysfunction. Worse still, these shots failed at their only claimed purpose—providing immunity. Breakthrough infections exploded, proving these were never vaccines, but a dangerous, unstable genetic weapon system masquerading as medicine.

The damage is irreversible for countless victims. A mere withdrawal of these shots is not enough. We demand full judicial accountability—criminal prosecutions for those who pushed this atrocity, a new compensation system for the injured, and the complete dismantling of the corrupt regulatory bodies that allowed this.

The COVID vaccine scandal is one of the greatest medical crimes in history. Those responsible must pay. Medical freedom is non-negotiable—never again.

Sources include:

ChildrensHealthDefense.org

Regulations.gov

ChildrensHealthDefense.org