FDA Authorizes First At-Home Test to Detect Both COVID-19 and Flu
The U.S. Food and Drug Administration (FDA) has authorized the first over-the-counter (OTC) at-home test for both the ...
Source: theepochtimes.com
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COVID-19: Recall Issued For Brand Of Rapid Tests That Could Produce Inaccurate Results
A manufacturer has recalled more than 56,000 COVID-19 rapid tests because they could produce inaccurate results.Universal Meditech Inc. issued the recall for Skippack Medical Lab antigen tests because they were distributed w…
Source: dailyvoice.com
COVID-19: Recall Issued For Brand Of Rapid Tests That Could Produce Inaccurate Results
A manufacturer has recalled more than 56,000 COVID-19 rapid tests because they could produce inaccurate results.Universal Meditech Inc. issued the recall for Skippack Medical Lab antigen tests because they were distributed w…
Source: dailyvoice.com
FDA Announces Recall of Tens of Thousands of Unapproved COVID Test Kits
A recall was issued for more than 56,000 COVID-19 rapid tests last week because they were not distributed ...
Source: theepochtimes.com
Ground News - COVID-19 antigen tests recalled over potential for inaccurate results
More than 56,000 COVID-19 antigen rapid tests are being recalled because they may provide inaccurate results, according to federal health officials.
Source: ground.news