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 Food and Drug Administration issued a new warning for users of certain CPAP machines – the latest in a series of troubles for Philips Respironics, one of the leading manufacturers of the breathing ...
Amsterdam, the Netherlands – Royal Philips (NYSE: PHG; AEX: PHIA) today announced an update in connection with the June 14, 2021 recall notification* for specific Philips sleep and respiratory care ...
GREEN BAY, Wis. (WBAY) - If you or someone you know suffers from sleep apnea, federal officials are warning about a device used to treat it. The FDA says if you have a Dream Station 2 made by Philips ...
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 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 ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback