by Brenda Baletti, Ph.D., Childrens Health Defense:
A growing chorus of voices among public health officials, scientists and researchers say there is sufficient scientific evidence to support an FDA Class I recall of COVID-19 vaccines. So far, the agency hasn’t responded to calls for either a moratorium or recall.
“It’s time for a recall” of the COVID-19 vaccines, epidemiologist Nicolas Hulscher argued on a recent episode of “Brannon Howse Live.” The mounting evidence that the COVID-19 vaccines caused death and other serious injuries are grounds for “Class I recall” by the U.S. Food and Drug Administration (FDA), Hulscher said.
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Hulscher is one of the growing chorus of voices among public health officials, scientists and researchers demanding public health officials hit the pause button on the shots until definitive safety studies are performed.
The latest round of calls began in January when Florida Surgeon General Joseph Ladapo called for a “halt in the use of COVID-19 mRNA vaccines” over safety concerns that the mRNA technology is delivering DNA contaminants into people’s cells.
A few weeks later, the journal Cureus published the first peer-reviewed paper to call for a moratorium on the COVID-19 vaccines. The paper included a sweeping review of “lessons learned” from the clinical trial data and the many adverse events associated with the shots.
Just last week, elected officials, organizations — including the World Council for Health and Door to Freedom — and hundreds of doctors and researchers sent a letter to the heads of state of 10 European countries calling for a suspension of the “modified mRNA vaccines,” citing serious health concerns associated with the shots.
Calls for a moratorium or a recall have been widely controversial. Ladapo was accused by The New York Times of peddling “misinformation.” The Washington Post said he had a pattern of making “debunked claim[s],” and FactCheck.org accused him of relying on “faulty science.”
Cureus retracted the “lessons learned” paper in what co-author Dr. Peter McCullough called, a “stunning act of scientific censorship.” The paper was later republished in two parts in a different peer-reviewed journal.
Despite efforts to censor and discredit medical professionals and researchers who draw attention to the harms associated with the vaccines, even mainstream publications have conceded that the COVID-19 vaccines can cause serious injuries and that vaccine-injured people have been ignored. Yet, they continue to push the shots.
Hulscher told The Defender that the mainstream media’s refusal to seriously report on calls to pull the vaccines from the market has serious implications for public health. It’s “a contributing factor to excess mortality” among global populations, he said.
“The FDA has failed to protect Americans from unsafe products because they suffer from corporate capture,” he added.
M. Nathaniel Mead, lead author of the “Lessons Learned” paper, told The Defender the FDA never should have authorized the vaccines in the first place. The “usual safety testing protocols and toxicology requirements were bypassed” and a reanalysis of the trial data showed serious adverse effects. “The ‘safe and effective’ narrative has always been a farce,” he said.
Freedom of Information Act requests have uncovered evidence that top officials at the FDA and Centers for Disease Control and Prevention knew about COVID-19 vaccine injuries early in 2021 — long before making the information public.
Still, U.S. public health agencies continue to authorize and recommend new boosters.
The FDA could easily respond to calls to halt vaccination, Hulscher said, by issuing a Class I recall, where a drug is recalled because it is likely that its use will cause serious health consequences or death — which he said nine studies and the Vaccine Adverse Event Reporting System (VAERS) data show.
“Because criteria for a Class I recall have been far exceeded, it should be an easy and effective way to halt the COVID-19 injection program and begin the process of compensating those who were harmed.”
Hulscher said he expects that calls will grow to withdraw the vaccines from the market until the regulatory authorities finally take action.
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