The Innova SARS-CoV-2 Antigen Rapid Qualitative Test, the CDC’s benchmark COVID diagnostic testing system, will be withdrawn for Emergency Use by the end of 2021 due to an inordinate frequency of false positive and negative results.
“The FDA has identified this as a Class I recall, the most serious type of recall. Use of these devices may cause serious injuries or death,” the FDA stated on its website.
Related
https://www.cdc.gov/csels/dls/locs/2021/07-21-2021-lab-alert-Changes_CDC_RT-PCR_SARS-CoV-2_Testing_
https://shore-215.blogspot.com/2020/10/we-are-being-lied-to-here-is-how.html
https://www.youtube.com/watch?v=aDC4XFs7LXc
https://shore-215.blogspot.com/search?q=pcr
George Soros & Bill Gates lead buyout of UK Covid testing company
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