The Food and Drug Administration (FDA) has issued a warning that the Abbott NOW™ point-of-care test to diagnose COVID-19 may potentially give inaccurate results. ...
The State Department of Health State Laboratories Division has distributed a total of 12 Abbott ID NOW COVID-19 rapid test instruments to all counties....
Abbott Laboratories announced on Friday, Mar. 27, that the U.S. Food and Drug Administration (FDA) has issued Emergency Use Authorization (EUA) for a new...