Nearly 5 million US adults who smoke and formerly smoked are now recommended for testing.
The US FDA is warning consumers and healthcare providers to not use the Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) because these tests are not authorized, cleared, or approved by the FDA.Read More
Mesa Biotech is recalling the Accula SARS-CoV-2 Test because certain lots of the test have an increased risk of giving false positive results due to contamination at the manufacturing facility, according to an FDA alert.Read More
While rapid antigen COVID tests remain a useful tool for the detection of COVID-19 infections, continuous assessment and updating is likely needed in the context of variants of concern.Read More
UVA Health researchers say they have developed a better way to predict the risk of COPD for people of non-European ancestry.Read More
The MEDQOR Podcast Network is joined by RT Paul Nuccio to discuss lung imaging technology, specifically the use of lung ultrasound for identifying and managing lung diseases.Read More
The US FDA is warning people not to use the E25Bio COVID-19 Direct Antigen Rapid Test (DART), according to an agency alert.Read More
The Siemens Healthineers CliniTest Rapid COVID-19 Antigen Self-Test is now available in the United States. The test received FDA authorization in January 2022.Read More