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 ...
(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 ...
SAN DIEGO, CA. - ACON Laboratories, Inc. announced that they would be recalling their “FlowflexSARS-CoV-2 Antigen Rapid Test (Self-Testing)” from American markets, according to the FDA. The ...
The FDA announced the recall of Flowflex SARS-CoV-2 Antigen Rapid Tests (Self-Testing). The tests are not authorized for sale in the U.S. They have only been cleared for Europe and other markets. The ...
The manufacturer of the “Flowflex COVID-19 antigen home test, which is approved for emergency use authorization in the U.S., said it discovered counterfeit Flowflex SARS-CoV-2 antigen rapid test (self ...