Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.
Philips Respironics has removed certain DreamStation devices due to programming errors that can result in failed therapy modes, according to the U.S. Food and Drug Administration.
Here are four of the latest recalls and corrections reported to the FDA.
HYDERABAD: Ballari, long plagued by inadequate healthcare, is witnessing a transformation thanks to NMDC’s Corporate Social ...
NOW has launched rtNOW Engage, a suite of turnkey service lines to support durable medical equipment (DME) companies, including follow-up checks for non-invasive ventilation (NIV) and BiPAP patients ...
Dublin, Aug. 26, 2025 (GLOBE NEWSWIRE) -- The "Respiratory Care Devices Market by Product (PAP Devices, Ventilators, Humidifiers, Oxygen Concentrators, Spirometers, Peak Flow Meter, Masks), Disease ...
Roy Jakobs, who joined Philips in 2010 and became CEO in 2022 amid a major crisis, has since played a key role in stabilizing ...
Nyxoah announced today that it filed a lawsuit against Inspire Medical Systems alleging the infringement of sleep apnea ...
(MENAFN- GlobeNewsWire - Nasdaq) The global respiratory care devices market is projected to grow from USD 23.6 billion in 2025 to USD 33.6 billion by 2030, with a CAGR of 7.3%. This growth is driven ...
In an era of heightened health awareness, a silent epidemic continues to affect millions worldwide: sleep-disordered breathing. This umbrella term for a group of conditions characterized by abnormal ...
One of the questions frequently asked is whether the government will replace CGHS with another insurance-based scheme under the 8th Pay Commission. We will understand the current situation in this ...
NMDC’s Corporate Social Responsibility initiative has modernized Ballari Medical College and Research Centre with advanced ...
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