Saturday, June 27, 2020

Jesus Tapdancing Christ*


Federal officials failed to immediately stop the distribution of many COVID-19 antibody tests they knew were flawed, leading to inaccurate data about the spread of the virus. Congress is now investigating why the FDA did not review the tests it allowed to be distributed widely throughout the U.S. Sharyn Alfonsi's three-month investigation into the faulty tests will be broadcast on 60 Minutes, Sunday, June 28 at 7 p.m. ET/PT on CBS.

COVID-19 diagnostic kits were in short supply when the pandemic broke out. An alternative test to detect the presence of antibodies in blood was sold as a way to indicate who was exposed to the virus at some point and could now be immune. Such tests would help officials track the disease and determine when it might be safe to begin opening up the economy. The FDA said it would allow the antibody tests to enter the US market and would do so without a formal review. Over 200 companies hit the market with the tests.

[...]

It took 50 days for the FDA to reverse its course on antibody tests. In May, it began requiring test developers to apply for emergency authorization and submit data to show their tests worked. It was too late, says Rep. Raja Krishnamoorthi. He is investigating the FDA for not regulating the antibody tests. "Fraudulent tests flooded the market. Hundreds and hundreds of tests taken by hundreds of thousands, if not millions of people," says the Illinois Democrat. All companies had to do to get their tests to the U.S. market was state they were self-validated.

[...]

It took almost three months before the FDA started pulling tests off the market, but by then, many American municipalities had already used the tests to determine whether they could send essential workers like EMTs, policemen and firemen back to work.

  CBS
Where would that 25th amendment be useful if not with this asshat in the oval?  Surely if he "wins", they'll pull it out.

Flip the Senate!

*h/t Kevin Kruse

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