More of these lawsuits need to happen.
Watts Family Sues DOD For Willful Misconduct in Groundbreaking COVID Vaccine Case
The family of George Watts, Jr.
“who died unexpectedly,” is suing the DOD, claiming “willful misconduct” because the DOD allegedly misled the public about the safety of the vaccine,
according to The Defender, a publication of the Children’s Health Defense (CHD).
According to the
lawsuit, the Report of Death Investigation from the Bradford County Coroner’s Office “clearly document[ed] Mr. Watts’ vaccine-induced death and the proximate causal connection,” calling the “Primary Cause” of death “COVID-19 vaccine-related myocarditis.”
Watts received two doses of Pfizer vaccines, “an unlicensed product produced under the auspices of the DOD,” according to the lawsuit. The
obituary and VAERS report below show the details of Watts’ deadly reaction to the mRNA vaccine.
The groundbreaking case contends the DOD rushed production under
Operation Warp Speed (OWS) “while engaging in a deliberate and calculated mass-deception campaign specifically designed to obfuscate the fact that OWS’ vaccines weren’t licensed “safe and effective,” was merely experimental, and legally could only be characterized as “maybe effective” but could not be pronounced safe,” according to the
lawsuit. The lawsuit notes that OWS was later transitioned to HHS and was “renamed HHS-DOD COVID-19 Countermeasures Acceleration Group (CAG).”
According to the lawsuit, the DOD “intentionally blurr[ed] the line of the critical distinction between ‘licensed’ and ‘experimental,” and therefore “duped millions of Americans” into participating in the “largest medical experiment” in “modern history.”
More specifically, the lawsuit centers around the simultaneous licensing of the
“interchangeable” Pfizer
Comirnaty COVID vaccine while extending the Emergency Use Authorization (EUA) for the Pfizer-BioNTech vaccine. According to a
Sept. 7, 2021, article in The Defender, the FDA violated federal law, pulling a “classic bait and switch” when it licensed
Comirnaty. According to the lawsuit, Pfizer originally “formally received an Emergency Use Authorization (“EUA”) from the FDA for its unapproved medical product on Dec. 11, 2020.”
An earlier
lawsuit filed by CHD in August 2021 alleges the
FDA effectively duped the public into believing they were taking a safer “licensed” vaccine (Comirnaty) when in fact, it was the experimental Pfizer-BioNTech EUA vaccine they were receiving. The distinctions are grounded in law and are important.
The EUA designation
authorizes “medical products for use in emergencies,” and those products may be used only when “there is no adequate, approved and available alternative to the product for diagnosing, preventing or treating such disease or condition.” Importantly, EUA-authorized drugs exempt drug manufacturers from legal liability. Moreover, few Americans knew Comirnaty was not available in the U.S. then. Only
small quantities of the licensed vaccine became available in the U.S. in August 2022.
The confusion over Comirnaty may have tricked people like Watts into taking “two injections of the unlicensed Pfizer-BioNTch COVID-19 vaccine”—injections that may have ultimately caused his death. Sadly, according to The Defender article, Watts “waited for a vaccine he thought was
‘safe and effective.'”
........More in the link
