WASHINGTON — A device made by Philips Respironics for treating sleep apnea should be monitored closely when in use because it can overheat, according to federal regulators. The Food and Drug ...
The U.S. Food and Drug Administration on Friday announced the recall of certain Philips Respironics devices designed to help people with breathing conditions keep breathing at a regular rhythm. The ...
The U.S. Food and Drug Administration (FDA) is warning that Philips Respironics continuous positive airway pressure (CPAP) machines, which are used to treat obstructive sleep apnea, should be ...
Millions of people across the country were jostled awake this year over fearful news: A critical device they were prescribed and relied on each night for sleep was suddenly labeled a hazard to their ...
Please provide your email address to receive an email when new articles are posted on . The FDA designated the recall of Philips Respironics DreamStation devices as class I. The devices are used in ...
FORT WORTH (CBSNewsTexas.com) — A massive recall of millions of sleep apnea machines that has dragged on for nearly two years has left many patients waiting with seemingly no good options. In June of ...
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