FDA YANKS COVID SHOTS — Emergency Use Authorizations RESCINDED After Years of Tyranny, Mandates, and Lies

The Food and Drug Administration has officially rescinded the Emergency Use Authorizations (EUAs) for the COVID-19 vaccines, the authorizations that were used to justify medical mandates, lockdowns, and mass coercion under Joe Biden’s failed regime.

The announcement was made Wednesday as the FDA simultaneously approved updated Covid boosters while ending the blanket “emergency” status that Big Pharma and government bureaucrats clung to for years.

The news came from Health and Human Services Secretary Robert F. Kennedy Jr., who posted the bombshell announcement on X.

The FDA has now granted standard marketing authorization, not emergency approval, for limited populations: Moderna (ages 6+ months), Pfizer (ages 5+), and Novavax (ages 12+). Americans may still access the vaccines if they wish, but only after consultation with their doctors.

RFK Jr., fulfilling a major campaign promise of President Donald Trump’s administration, made it clear that the era of unchecked mandates is over:

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for Covid vaccines, once used to justify broad mandates on the general public during the Biden administration, are now rescinded.

FDA has now issued marketing authorization for those at higher risk: Moderna (6+ months), Pfizer (5+), and Novavax (12+). These vaccines are available for all patients who choose them after consulting with their doctors.

The American people demanded science, safety, and common sense. This framework delivers all three.”

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

In July, the U.S. Food and Drug Administration (FDA) under the Trump administration formally updated the safety labeling on all mRNA COVID-19 vaccines to reflect what many Americans have been warning about for years: a disturbingly high risk of myocarditis—particularly in young men—and the possibility of long-term, irreversible heart damage.

The revised warnings apply to both Pfizer’s Comirnaty and Moderna’s Spikevax vaccines and follow months of mounting pressure over transparency and accountability regarding the true risks of these experimental injections.