When the U.S. Food and Drug Administration announced Aug. 23 it had granted full approval to the first Covid “vaccine” under the brand name Comirnaty, the mainstream media immediately ran with the narrative. Joe Biden jumped in front of a microphone and told businesses they needed to “step up” the mandating of vaccines for their employees.
Dr. Anthony Fauci told national media outlets he expected a whole host of new “mandates” to be fueled by the “approval” of the Pfizer jab.
There’s only one problem. The “approval” given by the FDA was not for the Pfizer jab currently available in the U.S. market.
The devil is always in the details. Some of us weren’t fooled.
See our article, which has over the past three days received nearly 150,000 reads: FDA ‘playing bait and switch’ with Americans, tricking them into believing shots currently being offered have been granted full approval when they have not.
But because we and a few others looked beneath the facade and checked the facts of what the FDA actually did and not what the media and Joe Biden’s administration said it did, we took some heat. Even some of our own subscribers questioned whether maybe we got it wrong.
No, it was the corporate media who got the story wrong. And as a result, thousands of Americans no doubt capitulated and went ahead and rolled up theirs sleeves, thinking they had no other choice legally than to succumb to their employers’ mandates.
Today, on Aug. 27, the Orlando, Florida-based Liberty Counsel, perhaps the most respected Christian legal firm in the nation, issued a press release that confirms our story.
Below is the release, published in full from Liberty Counsel.
WASHINGTON, D.C. – The Food and Drug Administration (FDA) has done a bait and switch by announcing it approved its “first COVID-19 vaccine” in order to push the “vaccine” mandates and protect the Pfizer pharmaceutical company from legal liability. However, there is currently no fully licensed COVID shot on the United States market.
Albeit confusing, and probably intentionally so, this summarizes the current status of the Pfizer-BioNTech shots:
- All existing Pfizer vials (in the hundreds of millions), remain under the federal Emergency Use Authorization (EUA) (meaning people have the “option to accept or refuse”);
- The third or “booster” Pfizer shot is identical to the above and remains under the EUA with limited use to certain categories of people;
- BioNTech received FDA approval for people ages 16 and above under the name Comirnaty, but there are no Comirnaty doses available in the United States;
- In other words, there is currently NO FDA approved COVID-19 injection available anywhere in the United States. Every COVID shot in America remains under the EUA law and thus people have the “option to accept or refuse” them; and
- Even when an FDA approved COVID shot becomes available, individuals are protected by federal law and many states laws from being forced to get these shots based on their sincere religious beliefs or conscience rights.
On August 23, the FDA issued two separate letters for two separate injections. There are now two legally distinct (Pfizer vs. BioNTech), but otherwise identical products.
The first letter is regarding FDA’s biologics license application approval for the Pfizer Inc/BioNTech COVID-19 injection which has been named Comirnaty. Yet Pfizer has not started manufacturing or labeling this drug for U.S. distribution, so it is not even available in the U.S. It is unclear whether or not it is protected by a liability shield, but web-based U.S. government communication indicates that the same program that provides compensation for COVID vaccine-related injuries will apply Countermeasures Injury Compensation Program (CICP) rather than the National Vaccine Injury Compensation Program). At this point, there apparently has been no compensation paid to people injured by one of the COVID shots via the CICP.
The Pfizer injection, on the other hand, is…