The Wuflu, Kung Flu scam continues. Infection rates, death rates, vaccinations, survivability, and so on have ALL been manipulated.
Check out my video that PROVES this nonsense is all about money.
In the meantime, here is the latest in yet another part of the scam: testing.
The US Food and Drug Administration (FDA) issued its second Class 1 recall (the most serious recall the FDA uses) of a COVID-19 test. And this is NOT the first recall.
This latest recall comes less than two weeks after the FDA recalled another COVID-19 test for similar issues.
The first recall occurred May 28, 2021. That warning applied to COVID-19 tests sold by Lepu Technology without authorization (See FDA Issues Public Safety Communication Warning Public and Healthcare Providers About COVID-19 Tests Sold By Lepu Technology).
Next, on June 10 of this year the FDA issued the second and most recent Class 1 recall for COVID-19 testing. Subsequently, the FDA provided a letter to the public and to healthcare providers, warning them to immediately stop using the affected tests. This particular warning affected the Innova SARS-CoV-2 Antigen Rapid Qualitative Test.
The FDA cited multiple reasons for issuing the warning and recall, including the fact that the test’s performance was not adequately established; the fact that the test had not yet received authorization; and concerns that the data provided by the Innova Medical Group with their emergency use authorization (EUA) application appeared to be copied from data provided by other test manufacturers.
The FDA warns that the Innova SARS-CoV-2 Antigen Rapid Qualitative Test is sold under many names, including:
- Innova COVID-19 Self-Test Kit (3T Configuration)
- Innova SARS-CoV-2-Antigen Rapid Qualitative Test (7T Configuration)
- Innova SARS-CoV-2-Antigen Rapid Qualitative Test (25T Configuration)
The FDA recommends that healthcare providers who have used the Innova SARS-CoV-2 Antigen Rapid Qualitative Test retest any patients who may have experienced an inaccurate result.
In short, you could have had a cold or flu and the test got it wrong.
Look at what is on the FDA’s site for what could go wrong.
Potential Risk of False Results
The Innova Medical Group SARS-CoV-2 Antigen Rapid Qualitative Test claimed to determine if a person had an active COVID-19 infection using a nasal swab sample and test strip. The Innova Medical Group SARS-CoV-2 Antigen Rapid Qualitative Test, however, does not have authorization, clearance, or approval from the FDA. In addition, the FDA has significant concerns that the performance of the Innova Medical Group SARS-CoV-2 Antigen Rapid Qualitative Test device has not been adequately established, presenting a risk of false results.
- False-negative results may lead to delayed diagnosis or inappropriate treatment of SARS-CoV-2, which may cause patient harm including serious illness and death. False-negative results can also lead to further spread of the SARS-CoV-2 virus, including when presumed negative patients are grouped into cohorts in healthcare, long-term care, and other facilities based on false test results.
- False-positive results could lead to a delay in both the correct diagnosis and the initiation of an appropriate treatment for the actual cause of patient illness, which could be another life-threatening disease that is not SARS-CoV-2. False-positive results could also lead to further spread of the SARS-CoV-2 virus when presumed positive patients are grouped into cohorts based on false test results.
In other words, regardless of results you may not know if you have Wuflu. Think about that for a moment.
Have you ever gotten a flu and NOT known you were sick? But you could have no symptoms for Wuflu and test positive or negative.
What a FARCE!
Who’s going to refund the taxpayers our money back for this bogus research? I could have created a test that yielded those results for a fraction of the price of Innova.
How Americans haven’t revolted against this nonsense is beyond me.