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Bubbles101

1,033 Posts.

241

13/10/21

16:05

Post #: 56772271
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Originally posted by jortexx: ↑

“
Level: Laboratory Alert

After December 31, 2021, CDC will withdraw the request to the U.S. Food and Drug Administration (FDA) for Emergency Use Authorization (EUA) of the CDC 2019-Novel Coronavirus (2019-nCoV) Real-Time RT-PCR Diagnostic Panel, the assay first introduced in February 2020 for detection of SARS-CoV-2 only. CDC is providing this advance notice for clinical laboratories to have adequate time to select and implement one of the many FDA-authorized alternatives.”

“CDC encourages laboratories to consider adoption of a multiplexed method that can facilitate detection and differentiation of SARS-CoV-2 and influenza viruses. ”

https://www.cdc.gov/csels/dls/locs/...-Changes_CDC_RT-PCR_SARS-CoV-2_Testing_1.html

none of this would be an issue if there were no issues with PCR picking up influenza.

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It's obvious you still didn't read the article I gave you.

Here's another one.

https://www.nebraskamed.com/COVID/pcr-test-recall-can-the-test-tell-the-difference-between-covid-19-and-the-flu
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