Hamilton Medical Recalls Breathing Circuit Set
Hamilton Medical issued a recall for certain coaxial breathing circuit sets used with C1, T-1, and MR1 ventilators, ordering them removed from where they are used or sold, according to an FDA alert.
Hamilton Medical issued a recall for certain coaxial breathing circuit sets used with C1, T-1, and MR1 ventilators, ordering them removed from where they are used or sold, according to an FDA alert.
Baxter has recommended removal of certain Duo-Vent solution sets used for administration of fluids to the patient's vascular system.
HHS secretary Robert F Kennedy, Jr signed determinations to end COVID-19 emergency use authorizations for drugs, biological products, and medical devices because the emergency circumstances no longer exist.
From assessing hypoxia and supplemental oxygen needs in respiratory patients to screening obstructive sleep apnea and evaluating dental sleep appliances, overnight pulse oximetry (OPO) offers noninvasive, cost-effective monitoring, as new technologies further streamline care.
Baxter issued an Urgent Medical Device Correction notice for all Volara System patient circuits to be corrected prior to continued use, according to an FDA alert.
Pediatric pulmonary rehab programs enhance exercise capacity, strength, and quality of life even when lung function measurements remain stable.