What’s preventing ALL federal judges and elected legislators from associating EUA Covid-19 medical mandates with coerced consent, by citing Nuremberg Codes, and having all the perpetrators tried, and hung?
If that was good enough for the Third Reich, why not the Fourth?
(Ethan Huff) U.S. Federal District Judge Allen Winsor of the U.S. District Court for the Northern District of Florida has ruled that Pfizer-BioNTech’s Wuhan coronavirus (Covid-19) “vaccine” bearing emergency use authorization (EUA) is not interchangeable with the company’s new Comirnaty injection, which was fully licensed by the U.S. Food and Drug Administration (FDA) back in August.
Since the two injections contain different ingredients and are manufactured in different ways, Judge Winsor said that they are legally not the same, and that the EUA one cannot be forced on people by the Department of Defense (DOD).
Judge Winsor did, however, reject a preliminary injunction requested by 16 service members against the U.S. military’s Chinese Virus injection mandate. A hearing for that case is scheduled for Sept. 14, 2022, which is nearly 10 months down the road.
Judge Winsor’s decision about the EUA injection from Pfizer-BioNTech also applies to those from Moderna and Johnson & Johnson (Janssen), both of which are also not approved or licensed by the FDA.
It turns out that the FDA’s approval of Comirnaty was accompanied by confusing documents and equally confusing public statements that did not specify any differences between the two injections.
“The licensed vaccine has the same formulation as the EUA-authorized vaccine and the products can be used interchangeably to provide the vaccination series without presenting any safety or effectiveness concerns,” one such confounding statement read.
“The products are legally distinct with certain differences that do not impact safety or effectiveness.”
The FDA utterly failed to explain how the licensed Comirnaty injection and the Pfizer-BioNTech EUA jab could “be used interchangeably,” despite having “certain differences” that make them “legally distinct.”
EUA drugs CANNOT be mandated under U.S. law
As explained by The Defender, EUA products are considered experimental under U.S. law. This means that they cannot be mandated, and everyone has the right to refuse them.
“?he Nuremberg Code, as well as federal law, provide that no human being can be forced to participate in a medical experiment,” The Defender further reported.
“Under 21 U.S. Code Sec.360bbb-3(e)(1)(A)(ii)(III), ‘authorization for medical products for use in emergencies,’ it is unlawful to deny someone a job or an education because they refuse to be an experimental subject.”
The FDA’s own fact sheet also says something similar, explaining that under an EUA, “it is your choice to receive or not receive the vaccine. Should you decide not to receive it, it will not change your standard medical care.”
Licensed vaccines can supposedly be pushed on employees and students, according to The Defender, however it is not explained how or why from a constitutional perspective.
Interestingly, the law further states that once a fully licensed product becomes available, in this case Comirnaty, none of the EUA products can continue to be administered. This means that the Biden regime and anyone else trying to force people to take any of these injections is a criminal.
Keep in mind that Comirnaty is not even available to the public yet. This means that there are no vaccines currently available that can legally be mandated on anyone.
“This EUA for the Pfizer-BioNTech COVID-19 Vaccine and COMIRNATY will end when the Secretary of HHS determines that the circumstances justifying the EUA no longer exist or when there is a change in the approval status of the product such that an EUA is no longer needed,” the FDA fact sheet explains.
Acting FDA commissioner Dr. Janet Woodcock said much the same thing about how the “black letter law is clear.”
“There can be no biologic license approved to a medical product for diagnosing, preventing or treating COVID-19 if there is also still an Emergency Use Authorization for the same medical product serving the same purpose,” she said.