Jiangsu Well Biotech Co. Ltd. on Wednesday recalled its COVID-19 Ag Rapid Test devices because they were distributed to U.S. customers without authorization, clearance or approval from the U.S. Food ...

The Food and Drug Administration announced Wednesday that a healthcare company has recalled 45,500 COVID-19 rapid tests due to a "high number of false positive reports." Pharmaceutical company ...

(KERO) — The U.S. Food and Drug Administration issued a "do not use' warning for three at-home rapid COVID-19 tests because the tests are not authorized, cleared or approved for use in the U.S. The ...

The Food and Drug Administration is warning consumers to avoid the use of three different types of COVID tests as they have not been authorized for use. The FDA announced in a statement that people ...

The Food and Drug Administration (FDA) on Tuesday named three unauthorized rapid COVID-19 tests that it says people should not use due to the risk of false results. The FDA instructed people to not ...

JERSEY CITY, N.J.--(BUSINESS WIRE)--Celltrion USA is voluntarily recalling two lots of Research Use Only DiaTrust COVID-19 Ag Rapid Test Kits because of the potential that they may be misused for ...

In a recent study posted to the Lancet preprint* server, researchers assessed the utility of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) rapid antigen testing (RAT) for patient triage ...