The race is on to get tested in light of the spreading Omicron variant but the FDA is warning against certain at-home antigen tests which have a high amount of false results. The LuSys Laboratories COVID-19 Antigen Test (Nasal/Saliva) and the LuSys Laboratories COVID-19 IgG/IgM Antibody Test haven't been authorized or approved for distribution or use in the U.S and according to reports have resulted in people receiving false results. If you have either of these tests, the FDA recommends not using it.
Any problems experienced with the tests can be reported on the FDA’s MedWatch Voluntary Reporting Form.
According to the FDA’s Tuesday warning, the LuSys Laboratories COVID-19 Antigen Test (Nasal/Saliva) and the LuSys Laboratories COVID-19 IgG/IgM Antibody Test have not been authorized or approved for distribution or use in the U.S.https://t.co/a3MPJ5PpKA