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 ...

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 ...

In partnership with Pittsburgh Post-Gazette. The massive recall of DreamStation machines and other breathing devices disrupted medical care for millions in the United States and around the world.

ProPublica is no longer taking submissions for this particular project, but you are welcome to contact us through our general tip form. Millions of Breathing Machines. One Dangerous Defect ProPublica ...

Dutch medical device maker Philips said Monday it had reached a $1.1 billion deal in the United States to settle lawsuits over faulty sleep machines in a case that have dogged the company. The company ...

Philips Respironics received thousands of complaints about a dangerous defect in its breathing machines but kept them secret for years as stock prices soared. The devices, including the popular ...