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 ...
The Food and Drug Administration (FDA) has cleared ACON Laboratories’ Flowflex COVID-19 Antigen Home Test, the first over-the-counter (OTC) antigen test. Previously, the test was authorized for ...
An example shared by the FDA comparing a counterfeit Flowflex COVID-19 Antigen Home Test with a real, FDA-authorized one. Food and Drug Administration Keep an eye out for counterfeit at-home COVID-19 ...
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 ...
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 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 ...
The Philadelphia Department of Public Health is recalling some at-home COVID-19 tests. Residents who got the Flowflex COVID-19 Antigen Home Tests are urged to check the lot numbers on the bottom of ...
More than 100,000 COVID-19 antigen test kits for at-home use have been found to be “not authentic” and have been recalled. The Philadelphia Department of Public Health said one lot of the Flowflex ...
ACON Laboratories explains how to spot the fake COVID-19 test in the U.S. market. The Flowflex SARS-CoV-2 Antigen Rapid Test (Self-Testing) kit isn’t authorized for sale in the United States. [ FDA ] ...
STATEN ISLAND, N.Y. — The U.S. Food and Drug Administration (FDA) is warning people to not use certain Flowflex coronavirus (COVID-19) rapid tests, because there is a risk of false results. The FDA ...
According to the agency, an extended expiration date means the manufacturer provided data showing that the shelf-life is longer than was known when the test was first authorized. For more information ...