A coronavirus antigen test has been recalled after officials discovered that it was a counterfeit and not approved by the Food and Drug Administration (FDA) for use in the United States. ACON ...

COVID-19 has crept back into southwest Ohio and northern Kentucky as two omicron subvariants have become the predominant strain of infection locally. But if you're looking to shake the dust off of ...

(WWTI) — The Food and Drug Administration has issued a recall on the “Flowflex™ SARS-CoV-2 Antigen Rapid Test.” According to the FDA, this test was first recalled in early January by ACON Laboratories ...

The Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing) kit isn’t authorized for sale in the United States. FDA ACON Laboratories wants U.S. consumers to use its “Flowflex COVID-19 Antigen Home Test ...

Flowflex introduces first US FDA-cleared 4-in-1 home test detecting RSV, Flu A/B and Covid for ages 6 months+: San Diego, California Tuesday, January 27, 2026, 09:00 Hrs [IST] ACO ...

According to the agency, an extended expiration date means the manufacturer provided data showing that the shelf-life is longer than was known when the test was first authorized. For more information ...

Another way people are ensuring the safety of themselves (and others): using rapid at-home Covid tests, to quickly check that everyone is coronavirus-free. But how do you find these home Covid-19 ...