Almost two full years into its Class I recall of more than 5 million respiratory devices, Philips has wrapped up safety tests covering nearly all of the affected models—and is reiterating its previous ...

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 ...

Hampton, NH – On March 1, 2024, Sleepnet Corporation initiated a worldwide recall for all CPAP and BIPAP masks with magnets due to potential interference with certain medical devices. When a magnet ...

Don’t you just want to hit the covers and have eight hours of uninterrupted sleep right after a stressful day at work? Unfortunately, this is a luxury that people with sleep apnea don’t get to revel ...

In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...

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 ...

If you've been diagnosed with obstructive sleep apnea (OSA), you know that a continuous positive airway pressure (CPAP) machine is supposed to be your best friend at bedtime. But for many of us, it ...

If your CPAP mask leaves you sore, leaking air, or waking up frustrated, you’re not alone. From better fitting techniques to clever accessories, small changes can make a huge difference in comfort and ...