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Every household in the United States now is eligible to order more free rapid COVID-19 test kits from the federal government.. Beginning Nov. 20, households that previously ordered tests this fall ...
T he US government has been helping people detect COVID-19 at home for several years with free COVID test kits delivered by the US Postal Service. On Sunday, March 9, the Department of Health and ...
Molecular kits are designed to detect the presence of COVID-19 earlier and more accurately than the antigen tests above. This kit contains one test. It's authorized for ages 2 and up.
The at-home test website includes information about at-home rapid testing, a video demonstration and FAQ on how to use the iHealth COVID-19 Antigen Rapid Test, and a link to place orders with the ...
Home COVID-19 test kits may not be as accurate with newer variants. By KCAL News Staff. May 31, 2022 / 4:48 PM PDT / KCAL News ... because antigen tests only detect the virus when it's contagious.
More than 56,000 COVID-19 antigen rapid test kits have been recalled because they were distributed without appropriate clearance or approval by the U.S. Food & Drug Administration.
Districts began receiving allotted test kits from Sonoma County Office of Education Thursday The Sonoma County Office of Education began distributing 160,000 rapid COVID-19 antigen test kits to ...
In December 2022, of 56,300 Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kits were recalled by Universal Meditech Inc. The products were distributed without appropriate premarket clearance ...
Flowflex COVID-19 Antigen Home Tests with the lot number COV2110012 have been recalled By Emily Rose Grassi • Published September 9, 2023 • Updated on September 9, 2023 at 6:08 pm Philadelphia ...
Three New Jersey pharmacies were penalized for selling COVID-19 antigen test kits that were not authorized for at-home use and for not properly displaying the price of the tests, the New Jersey ...
More than 56,000 COVID-19 antigen rapid test kits have been recalled because they were distributed without appropriate clearance or approval by the U.S. Food & Drug Administration.
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