FDA Revokes Emergency Authorization for Covid ‘Vaccines’ as Deaths Continue Surging

The U.S. Food and Drug Administration (FDA) has just revoked the federal government’s emergency authorization for Covid “vaccines” as deaths and deadly disease continue to surge among those who received the mRNA injections.

The move was ordered by the Department of Health and Human Services (HHS), now led by Secretary Robert F. Kennedy Jr.

HHS’s decision means that the Biden-era COVID-19 “emergency” has officially come to an end.

In a post on X, Kennedy announced:

“The emergency use authorizations for Covid vaccines, once used to justify broad mandates on the general public during the Biden administration, are now rescinded.”

The decision strips emergency clearance from roughly 240 million Americans, though Kennedy clarified:

“These vaccines are available for all patients who choose them after consulting with their doctors.”

I promised 4 things:

1. to end covid vaccine mandates.

2. to keep vaccines available to people who want them, especially the vulnerable.

3. to demand placebo-controlled trials from companies.

4. to end the emergency.

In a series of FDA actions today we accomplished…

— Secretary Kennedy (@SecKennedy) August 27, 2025

At the same time, the FDA approved limited use of updated shots from Pfizer, Moderna, and Novavax, but only for the elderly and individuals with risk factors for severe COVID-19.

The shift marks a stunning reversal after years of sweeping mandates and censorship of dissent.

Under federal law, emergency authorizations are meant only for products that “may be effective” in a crisis.

Standard FDA approval, in contrast, requires proof that a drug is “safe, pure, and potent.”

No such proof has ever been provided for mRNA injections, however.

FDA officials Dr. Marty Makary and Dr. Vinay Prasad warned earlier this year that the agency would no longer green-light shots for healthy young people without proper clinical trial data.

“The FDA can only approve products if it concludes, based on scientific evidence, that the benefit-to-harm balance is favorable,” Prasad said in May.

“And we simply need more data to have that confidence for younger individuals at low risk of severe disease.”

Meanwhile, uptake has collapsed.

As of April, just 13 percent of children and 23 percent of adults had received the most recent shots, according to U.S. Centers for Disease Control and Prevention (CDC) data.

The FDA decision comes after the CDC has now been forced to quietly launch a formal investigation into mRNA “vaccine” safety following years of mounting evidence of harm.

The agency confirmed the creation of a new COVID-19 Immunization Workgroup under its powerful Advisory Committee on Immunization Practices (ACIP).

The workgroup will be chaired by MIT professor Retsef Levi, a longtime critic of the CDC’s lack of transparency.

Levi is tasked with reviewing data on:

• Cardiovascular, thrombotic, neurological, and immunological harms.

• Risks from repeated booster doses, DNA contamination, and the persistence of spike protein in the body.

• Impacts on pregnancy, all-cause mortality, hospitalizations, and long-term disability.

The CDC admitted the probe will address “critical gaps” in scientific literature, including long-ignored concerns about impurities in the shots and how long the synthetic spike protein lingers in human tissues.

For years, critics were silenced as they raised alarms over injuries, fertility declines, and excess deaths.

Now, the agency is being forced to confront what it once dismissed.

Kennedy said the new policy fulfills four core promises: to end mandates, keep vaccines voluntary, require placebo-controlled trials, and “end the emergency.”

“The FDA actions accomplished all four goals,” he said.

With HHS pulling emergency powers and the CDC finally probing vaccine harms, the tide may be turning on one of the most controversial mass medical campaigns in modern history.

READ MORE – CDC Data Exposes Surge in Deaths Among Children of Covid-Vaxxed Mothers