FDA issues warning not to use specific COVID-19 test over risk of false results
The U.S. Food and Drug Administration has issued a safety communication warning people not to use the ACON Laboratories test named "Flowflex SARS-CoV-2 Antigen Rapid Test."
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Mar 2, 2022, 12:05 PM
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Updated 1,017 days ago
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14ds agoThe U.S. Food and Drug
Administration has issued a safety communication warning people not to use the
ACON Laboratories test named "Flowflex SARS-CoV-2 Antigen Rapid Test."
The test is packaged in a dark blue
box and has not been authorized, cleared, or approved by the FDA for
distribution or use in the United States.
The FDA is concerned about the risk
of false results when using this unauthorized test.
For more information, click HERE.
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