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 ...
A recall was issued for certain COVID-19 antigen rapid tests by Skippack Medical Lab for not being authorized for distribution in the U.S. The Class 1 device recall for Skippack Medical Lab SARS-CoV-2 ...
These rapid antigen tests offer a quick and easy way to screen for COVID-19, including the new variant EG.5, or "Eris" People / Madison Woiten Even if you’ve grown accustomed to a life without face ...
JURUPA VALLEY, Calif.--(BUSINESS WIRE)--GenBody America, LLC, the U.S. affiliate of GenBody, Inc., a South Korean manufacturer of rapid diagnostic tests and reagents for point-of-care applications for ...
Add Yahoo as a preferred source to see more of our stories on Google. Covid-19 at home Rapid Test Kit The FDA has extended the shelf life for some COVID-19 tests. Now that allergy season is here, many ...
(RTTNews) - LumiraDx Ltd. (LMDX), a diagnostics company, announced Friday that its rapid COVID-19 antigen assay, LumiraDx SARS-CoV-2 Ag Test has successfully received the Emergency Use Listing or EUL ...
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 ...
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