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.

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 ...

KNOXVILLE, Tenn. (WATE) — A Knoxville woman who suffers from sleep apnea is asking what does she do now after her CPAP machine has been recalled. Two months ago, the FDA recalled a group of continuous ...

(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,' ...