New Lung Cancer Screening Guideline Expands Eligibility
Nearly 5 million US adults who smoke and formerly smoked are now recommended for testing.
Nearly 5 million US adults who smoke and formerly smoked are now recommended for testing.
Approximately 500,000 tests—which the FDA has "significant concerns" of bacterial contamination—were distributed to CVS Health, as well as about 16,000 tests to Amazon.
BD received FDA emergency use authorization for its new molecular diagnostic combination test for SARS-CoV-2, Influenza A + B and respiratory syncytial virus (RSV).
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 MoreMesa 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 MoreWhile 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 MoreUVA Health researchers say they have developed a better way to predict the risk of COPD for people of non-European ancestry.
Read MoreCelltrion USA is recalling up to 311,000 affected POC DiaTrust COVID Rapid Tests because the tests may have been distributed to unauthorized users.
Read MoreResearchers at the University of Florida and National Yang Ming Chiao Tung University in Taiwan have developed a 30-second COVID test that can detect coronavirus infection in as sensitively and accurately as the gold standard PCR test.
Read MoreThe ATS and ERS have updated their pulmonary function tests technical standard series to address the uncertainty around the interpretation of tests.
Read MoreThe 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 MoreE25Bio is recalling its COVID-19 Direct Antigen Response Tests (DART) for several reasons, particularly that these tests were marketed and distributed to U.S. customers without authorization, clearance, or approval from the FDA.
Read MoreBase10 Genetics is recalling the RNAstill MTM specimen collection kits because they were distributed without proper premarket clearance from the FDA.
Read MoreThe US FDA is warning people not to use the E25Bio COVID-19 Direct Antigen Rapid Test (DART), according to an agency alert.
Read MoreThe Siemens Healthineers CliniTest Rapid COVID-19 Antigen Self-Test is now available in the United States. The test received FDA authorization in January 2022.
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