An at-home coronavirus test is being recalled by the FDA. The COVID-19 antigen and antibody test kits were distributed to pharmacies and sold directly to consumers

The Food and Drug Administration (FDA) has warned consumers to stop using an unauthorized COVID-19 at-home rapid test and antibody test over concerns that the kits may produce false results. The kits, produced by Lepu Medical Technology, were distributed to pharmacies to be sold to consumers for at-home testing and made available through direct sales despite not having FDA authorization.