Claim: The FDA announced that the CDC's PCR test for COVID-19 \u201cfailed its full review\u201d because it is "unable to differentiate between COVID and flu," resultin… WebJul 25, 2024 · If testing was performed more than two weeks ago and there is no reason to suspect current SARS-CoV-2 infection, it is not necessary to retest. Testing program organizers: Notify participants in your testing program to discontinue diagnostic use of these tests and to use an FDA-authorized test to continue testing. For listings of FDA …
Medical Device Recalls - accessdata.fda.gov
WebDec 13, 2024 · The U.S. Food and Drug Administration ( FDA) on Tuesday announced a COVID-19 test manufacturer is issuing a recall due to false test results. The COVID-19 tests were made by Detect Inc. and were sent to customers between July 26 and Aug. 26 of this year, according to the recall notice. WebJul 17, 2024 · In January, the FDA had alerted the public that Curative’s test could produce false results, causing people to possibly delay treatment and unknowingly spread the virus. Business COVID-19 turned ... introduction of journal example
CDC
WebOct 14, 2024 · “Either destroy the tests by placing them in the trash or return the tests using the FedEx return label that was included with the letter Innova sent to its customers.” The CDC released a statement in … WebDec 25, 2024 · The Innova SARS-CoV-2 Antigen Rapid Qualitative Test, the CDC’s benchmark COVID diagnostic testing system, will be withdrawn for Emergency Use by the end of 2024 due to an inordinate frequency of false-positive and negative results.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. WebJul 24, 2024 · The FDA’s second, more telling recall, highlights what the PCR’s creator, Nobel Prize winner Dr. Kary Mullis, warned us about.He stated the PCR test was meant … introduction of jupiter