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.

Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.

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 ...

Patients who use Philips’ DreamStation 2 continuous positive airway pressure (CPAP) machines should monitor them for signs of overheating, the Food and Drug Administration said in a Tuesday safety ...

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 ...

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 ...