Resmed Introduces Full Face Fabric CPAP Mask
Resmed announced the US introduction of its AirTouch F40, a fabric, full face CPAP mask option. It will be commercially available starting October 28, 2026.
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Resmed Introduces Full Face Fabric CPAP Mask
Resmed announced the US introduction of its AirTouch F40, a fabric, full face CPAP mask option. It will be commercially available starting October 28, 2026.
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FDA Clears Getinge Edi Catheter
The FDA granted 510(k) clearance to Getinge’s 6Fr/48 cm Edi catheter designed for premature infants weighing between 500 and 1,000 grams.
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Basic Cleaning Methods Decontaminated Single-Use Equipment
Basic washing techniques significantly reduced bacterial contamination on disposable equipment, offering potential emergency contingency options during critical supply shortages.
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Early Alert for React Health VOCSN Devices
Ventec Life (React Health) issued updated use instructions and inspection procedures for certain VOCSN ventilator devices, according to an FDA early alert.
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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.
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FDA Early Alert for Draeger Breathing Circuit
Draeger issued a letter to affected customers recommending certain VentStar Resus Neo hoses be removed from where they are used or sold, according to an FDA early alert.
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Early Alert for NOxBox Nitric Oxide Delivery System
NOxBox reported complaints of oxygen leaks due to failure of the oxygen tubing or tubing connection within the NOxMixer module of the NOxBoxi device, according to the FDA.
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Early Alert for CooperSurgical Neonatal nCPAP Device
CooperSurgical has issued a letter to affected customers recommending certain ventilators be removed from where they are used or sold, according to a USFDA early alert.
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Medline Recalls Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits
The FDA reports a nationwide recall of Hudson RCI Neonatal/Infant Heated Wire Breathing Circuits by Medline Industries.
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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.
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Sunset Healthcare Adds Pediatric NIV Mask Liners
Sunset Healthcare Solutions has added KidZzzs, the first mask liners pre-cut specifically for pediatric noninvasive ventilation (NIV).
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Products 2026: Resuscitation
RT looks at the latest resuscitation devices on the market from manufacturers like Dynarex, Fisher & Paykel Healthcare, Mercury Medical, and Zoll Medical.
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Products 2026: Intubation & Airway Management
A closer look at some of the latest airway management and intubation devices from Dale Medical, Karl Storz, Marpac, Medline Industries, Neotech Products, and Olympus.
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Products 2026: Airway Clearance & Suction
A closer look at suction and airway secretion clearance therapy devices from ABM, Baxter, Neotech, Sentec, Seoil Pacific, and Synchrony Medical.
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Products 2026: Gas Delivery & Humidification
The latest gas delivery devices including humidification, oxygen therapy and inhaled nitric oxide delivery from Airgas, Drive, Dynarex, Flexicare, Hans Rudolph, Linde, Neotech, Precision Medical, Salaera, and Southmedic.
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Products 2026: Ventilators & Critical Care Accessories
RT looks at the latest ventilation products from Breas, Draeger, Hamilton, Nihon Kohden, Solutions in Critical Care, and Sunset Healthcare.
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Drive Medical Launches Unbound IQ Brand
The new portfolio includes smart monitoring and cueing devices designed to support proactive patient care and data-driven insights.
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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.
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FDA Issues Early Alert for Resmed Ventilators
Resmed has recommended corrections to certain Astral 100 and Astral 150 ventilators due to an issue that may result in interrupted therapy.
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Lung Denervation Trial to Target COPD Phenotype
Nuvaira treated the first patient treated in a clinical trial evaluating a one-time lung denervation therapy for patients with specific COPD symptoms.
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HHS Ends COVID-19 Emergency Use Authorizations
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.
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Dynarex Launches POC, Neo/Pediatric Closed Suction Catheters
Dynarex Corp launched a new Resp-O₂ Portable Oxygen Concentrator and a new line of infant- and pediatric-sized closed suction catheters.
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FDA Clears Upgraded Software for Evita V800 Ventilator
Draeger Inc has received 510(k) clearance from the USFDA to market its 3.10 software for the Evita V800 ventilator, according to a company news release.
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FDA: Urgent Correction for Baxter Volara System
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.
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