Deaths reported to the CDC far exceed the recall limits of past vaccine withdrawals, with figures surpassing historical thresholds by as much as 375,340 percent.
More experts are calling for COVID-19 “vaccines” to be immediately withdrawn from the market after a new peer-reviewed study found irrefutable evidence that the shots cause harm.
The study, published in Science, Public Health Policy and the Law,1 asserts that deaths reported to the Vaccine Adverse Event Reporting System (VAERS) far exceed the recall limits of past vaccine withdrawals, with figures surpassing historical thresholds by as much as 375,340 percent. Additionally, the analysis found that mass COVID-19 vaccination campaigns have coincided with an alarming increase in mortality, adverse events, and risks that outweigh any perceived benefits.
Excess mortality, negative efficacy, and widespread DNA contamination associated with COVID-19 vaccines have been clearly established, and the U.S. Food and Drug Administration’s (FDA) criteria for a “Class I recall” have been “far exceeded,” the researchers said.
A Class I recall is the most severe type of recall issued by the FDA. It indicates that a product has a reasonable chance of causing serious injury or death. Historically, vaccines have been withdrawn from the market for far fewer reported deaths than those associated with COVID-19 vaccines.
For example, just two weeks after being hailed as “America’s gift to the world,” the inactivated polio vaccine (IPV) was pulled off the market after it infected more than 40,000 people with polio, left 250 children paralyzed, and resulted in 10 deaths. The Cutter incident of 1955 remains one of the most significant pharmaceutical disasters in history.
The 1976 swine flu vaccine was recalled after 53 reported fatalities, and the 1999 Rotashield vaccine was suspended after 15 cases of intussusception, a rare, serious condition in which one part of the intestine telescopes into another.
Yet when the study’s authors examined VAERS data from Sept. 6, 2024, the Centers for Disease Control and Prevention (CDC) recorded 19,028 U.S. deaths from COVID-19 vaccines reported by healthcare professionals or pharmaceutical companies who believed the product was associated with the death. Roughly 1,175 deaths occurred on the same day as vaccination, and 1,250 occurred the day following vaccination.
VAERS, co-managed by the CDC and FDA, is a national early warning system for monitoring the safety of vaccines after licensure. It is a passive surveillance system, meaning it relies on individuals to report adverse events voluntarily. This reliance can lead to underreporting, as not all adverse events are submitted to the system.
By Megan Redshaw
