| MedWatch - The FDA Safety Information and Adverse Event Reporting Program | | | Today, the U.S. Food and Drug Administration (FDA) posted an update to the SARS-CoV-2 Viral Mutations: Impact on COVID-19 Tests web page to share the latest information. The update added new information about a potential impact on the performance of the Mesa Biotech Inc. Accula SARS-CoV-2 Test due to a genetic mutation at positions 28877-28878 (AG to TC) in patient samples. Questions? If you have questions about this update, email COVID19DX@fda.hhs.gov | | | |
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