Early Alert for Baxter Duo-Vent Solution Sets
Baxter has recommended removal of certain Duo-Vent solution sets used for administration of fluids to the patient's vascular system.
Baxter has recommended removal of certain Duo-Vent solution sets used for administration of fluids to the patient's vascular system.
The FDA approved the first gene therapy for children as young as 2 years old with sickle cell disease or transfusion-dependent beta thalassemia.
The collaboration will focus on sleep and circadian medicine, including research into obstructive sleep apnea and wearable health technology.
Michelle Ng Gong succeeds Raed Dweik as president of the American Thoracic Society.
Perma Pure and Maxtec have unified under a new parent company, Salaera, to form a global technology platform for breath and gas systems.
Benralizumab (Fasenra) is now indicated to reduce the risk of flare ups for adult and pediatric patients with hypereosinophilic syndrome.
GE HealthCare has issued a letter to affected customers recommending Infant Resuscitation Systems and Warmers with a M1091607-R blender be corrected prior to continued use, according to an FDA alert.