The Food and Drug Administration yesterday alerted health care providers to a recall and change in reprocessing methods for certain urological endoscopes made by Karl Storz.
The House Energy and Commerce Subcommittee on Health today held a hearing on legislation to reauthorize federal mental health programs and support mental health and wellbeing.
The provision being challenged by AHA and AMA implicates the arbitration process for determining fair payment for services by out-of-network providers.
Hospitals and health systems, and their community and public health partners, are invited to share how they are overcoming challenges to make a positive difference during the COVID-19 pandemic.
Three more regions are no longer authorized to treat patients at high risk for progressing to severe COVID-19 with sotrovimab because the monoclonal antibody is unlikely to work against the BA.2 variant predominating there.