Lateral Flow Tests Innovas Iniquity

Posted on 28th September, 2021


"The United States Food and Drug Administration (FDA) told the public to stop using the [lateral flow] tests ‘by placing them in the trash’ ... Shockingly, the UK government decided to take no notice. Instead they doubled down on their £4billion investment in the product."


In an article by Conservative Woman:

"While Americans were busy throwing them in the trash, the UK extended the exceptional use authorisation (EUA) of the Innova LFT until August 28. (FDA Link)


It is now well past that August 28deadline and there has been no further official extension of the EUA by the MHRA. Yet schools, colleges and universities are once again strongly encouraging students to use these unauthorised lateral flow tests. As well as risking health, the test will continue to inflate case numbers as a result of its proven unreliability and inaccuracy and will be a ‘tool’ in the Prime Minister’s box of tricks to ‘justify’ yet another lockdown this autumn/winter." (Article and PDF)

Previous artticles include:

  • Innova’s iniquity, Part 1 How test firm flashed the UK taxpayer's cash (PDF)
    • "Revealed in the article is the critical fact that John Penrose MP, the Government’s anti-corruption champion, who ‘rather than chasing corruption … seems to spend his time besmirching those who do’ is the husband of Harding." ["Tory life peer Dido Harding head of NHS Test and Trace from May 2020 to May 2021"]
    • "This fact was found ‘laughable’ by Jolyon Maugham, chairman of GLP. I concur. How can an independent inquiry ever be launched if it is your own spouse you’re supposed to be investigating? This glaring conflict of interest has been shockingly ignored by the mainstream media."
  • Innova Scandal
    • Part 1 - The Innova lateral flow tests: another scandal in the making? (PDF)
    • Part 2  - The Innova lateral flow tests: another scandal in the making? (PDF)
    • Part 3 - The US says ‘Throw the tests in the trash’ (PDF)
    • Part 4 - Questions the government must answer (PDF)


See also:

  • FDA -
    • Innova Medical Group Recalls Unauthorized SARS-CoV-2 Antigen Rapid Qualitative Test with Risk of False Test 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" (PDF)
  • Lancet Comparision LFT vs PCR
    • Comparing the diagnostic accuracy of point-of-care lateral flow antigen testing for SARS-CoV-2 with RT-PCR in primary care (REAP-2) (PDF)
  • Related Blogs
  • COVID page
  • Global page
  • Beinvolved page





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