FDA: Reworked Philips Trilogy Ventilators Have Additional Safety Issues
The FDA reports that Philips Trilogy ventilators reworked as a part of the June 2021 recall have two new potential issues that may affect performance and safety.
The FDA reports that Philips Trilogy ventilators reworked as a part of the June 2021 recall have two new potential issues that may affect performance and safety.
Philips Respironics is recalling certain V60 and V60 Plus ventilators due to an expired adhesive in what the FDA has labeled a Class I recall.
The FDA has granted De Novo Clearance for the Philips CavaClear, an IVC Filter Removal Laser Sheath used to remove an IVC filter when previous methods of removal have failed, according to the company.
As patients await repaired or replaced CPAP devices, many turn to in-line filters that are readily available over the internet.
Read MoreA closer look at suction and secretion clearance devices from Philips Healthcare, Seoil Pacific, Neotech Products, and International Biophysics Corp.
Read MoreRT looks at the latest ventilators and critical care products on the market from manufacturers like Breas Medical, Dräger, Philips, Zoll, Hans Rudolph, and more.
Read MoreA look at oximetry and patient monitoring technology from Masimo and Capsule Technologies / Philips Healthcare.
Read MorePhilips has issued a recall in the United States, and a field safety notice for the rest of the world, for specific Philips bilevel positive airway pressure (bilevel PAP), CPAP, and mechanical ventilator devices.
Read MoreIn hospital settings, the terms “NIV” and “BiPAP” are often used synonymously. However, when patients are being discharged to home care, the exact terminology used by physicians is essential in order to prescribe the precise therapy.
Read MoreThe new facial scanning system analyzes each patient’s anatomy to recommend a more precise CPAP mask size.
Read MoreThe UK’s National COVID-19 Chest Imaging Database is a centralized database containing X-Ray, CT and MRI images from hospital patients across the country.
Read MoreRoyal Philips and healthcare-AI developer Orbita Inc will co-create next-generation conversational virtual assistants for Philips consumer health and patient support applications.
Read MoreRespiratory failure due to hypoxemia and/or hypercapnia calls for oxygen therapy, positive pressure support, and possibly ventilatory support. Care for these patients may escalate and require higher flow, FiO2, and more complex devices and intensive monitoring.
Read MoreRoyal Philips has completed the acquisition of BioTelemetry Inc, a leading US-based provider of remote cardiac diagnostics and monitoring.
Read MoreRetia Medical is the first company to utilize Capsule Technologies’ new Device Driver Interface (DDI) development strategy to integrate its Argos Cardiac Monitor.
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