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 ...
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 ...
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 ...
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 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 ...
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 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback