This could have made headlines the world over. The Facilities for Illness Management and Prevention quietly advised the US authorities to destroy all obtainable Janssen/Johnson & Johnson COVID-19 vaccines. “Janssen COVID-19 Vaccine is no longer available in the U.S. All remaining U.S. government stock of Janssen COVID-19 Vaccine expired May 7, 2023. Dispose of any remaining Janssen COVID-19 Vaccine in accordance with local, state, and federal regulations. Dispose of any remaining Janssen COVID-19 Vaccine in accordance with local, state, and federal regulations,” the location states. Over 19 million People obtained the Johnson & Johnson “secure and efficient” vaccine. The 12.5 million doses in storage are to be instantly destroyed. The well being company didn’t state why they had been pulling the vaccine.
On February 27, 2021, Johnson & Johnson boasted that the FDA approved the first single-shot vaccine. Nonetheless, the corporate admitted that 41% of those that participated within the vaccination research had comorbidities. The corrupt FDA nonetheless allowed it to be prescribed, realizing that nearly half of the research members had damaging unwanted effects. On the time of this writing, the Johnson & Johnson web site makes no point out of the vaccine recall. They’re centered on their constructive Q1 earnings report, nevertheless.
The hundreds of thousands of individuals all through the world who took this vaccine, by alternative or by drive, need to know the rationale it has been recalled. Within the US, the federal government supplied the pharmaceutical corporations full immunity so there can be no class-action lawsuit.
One can assume, based mostly on the CDC’s personal steering, that the single-dose vaccine elevated unwanted effects. The CDC states that check topics should wait 8 weeks between the primary and second mRNA jabs “as it would cut back the small threat of myocarditis and pericarditis related to these COVID-19 vaccines.” The positioning continues, “Whereas absolute threat stays small, an elevated threat for myocarditis and pericarditis has been noticed amongst mRNA COVID-19 vaccine recipients, notably in males ages 12–39 years. Instances of myocarditis and pericarditis had been recognized in scientific trials of Novavax COVID-19 Vaccine and thru passive surveillance throughout post-authorization use outdoors america.” Additionally they talk about the “small threat” of those lethal unwanted effects in kids aged 12 to 17.
The individuals ought to demand quick solutions. Solutions can be required instantly in the event that they had been producing something however the COVID-19 vaccination. Why did the FDA approve a vaccine that they knew to be harmful? Will they recall different vaccines with rising loss of life tolls? We deserve clear solutions.
The put up CDC Quietly Recalls all Johnson & Johnson COVID Vaccines in US first appeared on Armstrong Economics.
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