WebJan 9, 2024 · ACON Laboratories Issues a Recall of non-EUA Authorized “Flowflex™ SARS-CoV-2 Antigen Rapid Test (Self-Testing)” Tests From the U.S. Market Jan 9, 2024 WebMar 3, 2024 · Administration (FDA) recall. In early January, the FDA identified the U.S. distribution of unauthorized test kits with the trade name “Flow. flex. SARS-CoV-2 Antigen Rapid Test (Self-Testing),” and subsequently issued a recall as these tests have not been approved, cleared, or authorized by the FDA. ACON Laboratories is
HSA says COVID-19 ART kits sold in Singapore not affected by US …
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March 15, 2024 Communications Director …
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