An Open Letter to Robert F. Kennedy Jr. The HHS Secretary is legally obligated to take immediate action to recall the Pfizer and Moderna mRNA injectables because they “present an imminent or substantial hazard to the public health.”-JAMES ROGUSKI

[Nat Quinn]

December 29, 2024

Dear Robert F. Kennedy Jr.,

This open letter is written in support of your efforts to Make America Healthy Again.

In my humble opinion, you will NOT be able to Make America Healthy Again unless you convince President Donald J. Trump that Operation Warp Speed was a grave mistake.

The biological products licenses for the Pfizer and Moderna mRNA COVID-19 “vaccines” must be REVOKED, the mRNA injections must be RECALLED, they must be REMOVED from the children’s vaccine schedule and they must be taken off the market IMMEDIATELY.

As the Secretary of the Department of Health and Human Services, YOU will have both the lawful authority as well as an obligation to stop the carnage that these ill-conceived products have caused.

After your confirmation and IMMEDIATELY after taking the oath of office as the Secretary of the Department of Health and Human Services, I call upon you to exercise your authority and fulfill your obligations under the laws listed below to RECALL the Pfizer and Moderna mRNA “vaccines” because they present a documented, imminent and substantial hazard to the public health.

I also implore you to direct the FDA Commissioner to REVOKE the biological products licenses for Pfizer’s and Moderna’s “vaccine.” There are multiple reasons for which 21 USC § 601.5 enables the FDA to revoke the licenses for these products.

Please note the appropriate sections of the United States Code in Annex 2 attached to this letter.

Pfizer clearly failed to properly notify the FDA of a change in the manufacturing procedures from what has come to be known as “process 1” which was used to produce the biological products for the clinical trials. They switched to “process 2” in order to produce the biological products that have been injected into billions of people worldwide.

Both Pfizer’s and Moderna’s products have caused harm and death that far exceed the Bradford Hill criteria. Please watch the video below:

https://rumble.com/v4h2xwo-dr.-jessica-rose-phd-13-facts-on-covid-19-injections.html

Please remember that on May 16, 2021 you, along with Mary Holland and Dr. Meryl Nass, on behalf of your organization, Children’s Health Defense, submitted a Citizen Petition requesting that Janet Woodcock, the acting FDA Commissioner at the time, “revoke Emergency Use Authorizations for existing COVID vaccines and refrain from approving and licensing them.”

https://childrenshealthdefense.org/wp-content/uploads/FDA-2021-P-0460- 0001_attachment_1.pdf

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Please review the blatantly inaccurate and deceptive communication that Peter Marks, the Director of the Center for Biologics Evaluation and Research, sent to Florida Surgeon General Joseph Ladapo on December 14, 2023:

https://www.fda.gov/media/174875/download

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Please also be aware of these two letters from Senator Ron Johnson about the lack of transparency regarding the adverse events associated with the mRNA vaccines:

https://www.ronjohnson.senate.gov/services/files/00AAFB3D-72EE-475F-94D5- 66708B4AA86D

https://www.ronjohnson.senate.gov/services/files/FB6DDD42-4755-4FDC-BEE9- 50E402911E02

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Supportive evidence is available here:

https://publichealthpolicyjournal.com/biontech-rna-based-covid-19-injections-contain-large- amounts-of-residual-dna-including-an-sv40-promoter-enhancer-sequence/

https://www.ijvtpr.com/index.php/IJVTPR/article/view/101/341 (Part 1) https://www.ijvtpr.com/index.php/IJVTPR/article/view/104/359 (Part 2)

and here:

https://NotSafeAndNotEffective.com

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The current situation meets the criteria for a CLASS 1 recall:

Class I recall: 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.

https://www.fda.gov/safety/industry-guidance-recalls/recalls-background-and-definitions

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The Secretary of the Department of Health and Human Services has the authority to take action to protect the health of the American people when a biological product “presents an imminent or substantial hazard to the public health,” and is also OBLIGATED BY LAW TO TAKE ACTION:

“the Secretary [of the Department of Health and Human Services] SHALL issue an order immediately ordering the recall of such batch, lot, or other quantity of such product.”

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The most effective way for you to help Make America Healthy Again is to do everything in your power to remove the mRNA injectable products from the marketplace.

Failure to remove the mRNA COVID-19 “vaccines” from the marketplace will give the FALSE impression that the mRNA platform is “safe and effective” and will leave the door wide open for future development of additional mRNA “vaccines” that may result in similarly horrific results.

If you fail to act IMMEDIATELY, then every adverse event, every disability and every death that is subsequently caused by the mRNA injections will occur due to YOUR failure to take immediate action.

I encourage you to take action upon this matter as a top priority as soon as you take the oath of office as the Secretary of the Department of Health and Human Services.

God bless you.
God Bless America.
God bless all the people of the world.

Sincerely,

James Roguski

310-619-3055

 

SOURCE:An Open Letter to Robert F. Kennedy Jr. – James Roguski

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