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In a Facebook Live broadcast Thursday evening, DMLNewsApp and TeamDML.com founder Dennis Michael Lynch (DML) shared details of a newly released report stating the FDA is questioning the accuracy of coronavirus tests produced by Abbott.

WASHINGTON (AP) — Federal health officials are alerting doctors to a potential accuracy problem with a rapid test for COVID-19 used at thousands of hospitals, clinics and testing sites across the U.S., including the White House.

The Food and Drug Administration said late Thursday it is investigating preliminary data suggesting Abbott Laboratories’ 15-minute test can miss COVID-19 cases, falsely clearing patients of infection. The test is used daily at the White House to test President Donald Trump and key members of his staff, including the coronavirus task force.

The researchers found that Abbott’s test, run on the company’s portable ID NOW system, missed one-third of the infections caught by Cepheid’s test when swabs were stored in liquid used to transport laboratory samples. When the samples were kept dry the test missed 48% of the cases flagged by Cepheid’s test.

The researchers called the test’s performance “unacceptable,” due to the risk of falsely clearing patients who could spread the infection to others. They acknowledged shortcomings of the study, including the time needed to transport patient samples to the device for processing.

DML warned that this will be used as an excuse to try to keep the country shut down longer.

WATCH his full commentary on the report in the video below. (Scroll down for details on how to join the growing TeamDML.com movement!)

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