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 ...
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 ...
If you have an at-home COVID-19 Flowflex test that came in a dark blue box, don't use it, the US Food and Drug Administration said this month. At least, if you got it in the US. While the Flowflex ...
The warning is for the “Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing)” from ACON Laboratories. The test comes in a dark blue box with white lettering and symbols in the lower right corner of ...
A common rapid at-home COVID test has become the subject of a recent product recall over concerns the antigen test hasn't received proper U.S. authorization. The Food and Drug Administration issued a ...
Flowflex™ is a rapid test for the detection of SARS-CoV-2 antigens in anterior nasal specimens within 7 days of symptom onset or without any symptoms. This test is easy to use, accurate and is EUA for ...
The US Food and Drug Administration has granted an Emergency Use Authorization to an over-the-counter (OTC) COVID-19 test that agency officials say will double at-home testing capacity. The ...
ACON Laboratories, Inc. announced the retail availability of the first FDA-cleared home test which allows families to identify four major respiratory infections, including respiratory syncytial virus ...
SAN DIEGO, Jan. 23, 2026 /PRNewswire/ -- ACON Laboratories, Inc. today announced the retail availability of the first FDA-cleared home test which allows families to identify four major respiratory ...
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