Luna G3 APAP Recalled Due to Firmware Defect
According to an FDA alert, BMC Medical Co Ltd retrospectively reported a recall of 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to firmware defect.
According to an FDA alert, BMC Medical Co Ltd retrospectively reported a recall of 20,160 Luna G3 APAP (Model LG3600) devices distributed in the United States due to firmware defect.
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.
A closer look at suction and airway secretion clearance therapy devices from ABM, Baxter, Neotech, Sentec, Seoil Pacific, and Synchrony Medical.
Autonomous Healthcare received FDA De Novo marketing authorization for Syncron-E, a software that supports the assessment of patient-ventilator asynchrony by detecting evidence of ineffective efforts.
Resmed has recommended corrections to certain Astral 100 and Astral 150 ventilators due to an issue that may result in interrupted therapy.
Patients with long COVID receiving individualized cognitive rehab showed significantly higher goal attainment scores at three months compared to standard care.