Earlier this week, the U.S. Department of Justice, representing the Food and Drug Administration and healthcare technology company Philips came to an agreement to no longer sell their sleep therapy or ...

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 ...

The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...

Philips released the latest set of safety test results on Tuesday, covering all CPAP and BiPAP sleep therapy machines included in the recall—which together make up about 95% of all of the recalled ...

An initial report Philips issued in early September said the recall affected “more than 17 million” of certain masks used with CPAP and BiPAP machines, but the FDA now counts a total of 18,670,643 ...

Millions of CPAP sleep apnea machines made by the medical device maker Philips and a subsidiary were found to have a dangerous problem, triggering consumer lawsuits and a massive recall in 2021. Now, ...

Certain Philips Respironics DreamStation breathing devices, commonly used for treating sleep apnea, may deliver the incorrect prescription or no therapy at all, the FDA warned in a recall announcement ...

The U.S. Food and Drug Administration has updated a recall affecting millions of Philips sleep apnea machines, now saying that they may been linked to at least 561 deaths. The agency, in a statement ...

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,' ...

In Rochester, N.Y., Diane Coleman has relied on a machine to help her stay alive, but she worries that it might be slowly undermining her health. Her ventilator was among millions of breathing devices ...