Philips DreamStation 2 continuous positive airway pressure (CPAP) machines should be monitored for signs of overheating, according to the Food and Drug Administration (FDA). The Philips DreamStation 2 ...

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,' ...

The ongoing recall of millions of breathing devices made by Philips has been botched and belabored at nearly every turn: It took more than a decade after users first reported the soundproofing foam in ...

Philips DreamStation 2 continuous positive airway pressure (CPAP) machines for sleep apnea may overheat, according to an FDA safety alert on Tuesday urging patients to monitor their devices. "The FDA ...

The manufacturer, Philips Respironics, said it would compensate users of CPAP machines and other flawed devices that were recalled after they blew bits of foam into consumers’ mouths and lungs. By ...

Medical device maker Phillips formally entered into a consent decree that stops the company from selling sleep apnea machines in the United States over health concerns that include cancer. The decree ...

Please provide your email address to receive an email when new articles are posted on . Reports of fire, smoke, burns and other signs of overheating are emerging for DreamStation 2 CPAP machines by ...

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 ...