If you use a Philips CPAP machine, you have another thing to keep you awake at night: The FDA issued a warning Tuesday to patients and health care providers saying the company’s DreamStation 2 ...

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 ...

Three years after one of the largest medical device recalls in history, the fallout – health-wise and financial – continues to impact many patients with sleep apnea. Now a critical deadline is ...

The FDA said that it has received reports that the machines can overheat and cause “thermal issues such as fire, smoke, burns and other signs of overheating while people are using” the devices. The ...

In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...

A voluntary recall of millions of CPAP breathing machines, used mainly to treat sleep apnea, has many users wondering if they've been inhaling cancer-causing toxins in their sleep. At least 25 million ...

Medical equipment company Philips has issued a recall on some products to address possible health risks associated with a foam component meant to help reduce noise. The polyester-based polyurethane ...

(RTTNews) - Shares of Philips Electronics NV were losing around 5 percent in Amsterdam trading as well as in the pre-market activity on the NYSE after the U.S. regulator warned against the safety of ...

Orlando, Florida — Carrie Markham spent three years struggling to breathe, suffering from lung problems that began in March of 2020, puzzling her doctors. "They just kept saying, 'We just don't know,' ...

The FDA is warning patients and healthcare providers that it has received over 270 reports about Philips (NYSE:PHG) Respironics' DreamStation 2 CPAP machines overheating, which can lead to injury. In ...