The FDA announced today that the CDC PCR test for COVID-19 has failed its full review.
Its Emergency Use Authorization has been REVOKED.
It is a Class I recall. The most serious type of recall.
Too many false POSITIVES!
This is the test that started the pandemic.
The test used in all the nursing homes in Washington and New York.
This was the ONLY test in use until May of 2020. THE VACCINE CAUSES THE DELTA VARIANT! THIS IS THE SINGLE MOST HORRIFIC CRIME AGAINST HUMANITY SINCE THE DAWN OF MANKIND.
https://www.fda.gov/medica...
https://t.me/therightsidew...
Its Emergency Use Authorization has been REVOKED.
It is a Class I recall. The most serious type of recall.
Too many false POSITIVES!
This is the test that started the pandemic.
The test used in all the nursing homes in Washington and New York.
This was the ONLY test in use until May of 2020. THE VACCINE CAUSES THE DELTA VARIANT! THIS IS THE SINGLE MOST HORRIFIC CRIME AGAINST HUMANITY SINCE THE DAWN OF MANKIND.
https://www.fda.gov/medica...
https://t.me/therightsidew...
Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test Results | FDA
Innova SARS-CoV-2 Antigen Rapid Qualitative Test performance characteristics have not been adequately established, presenting a risk of false results.
https://www.fda.gov/medical-devices/medical-device-recalls/innova-medical-group-recalls-unauthorized-sars-cov-2-antigen-rapid-qualitative-test-risk-false-test
12:43 AM - Jul 25, 2021
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