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.

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 ...

I have used CPAP for almost two decades and I learned a number of useful things. I would strongly recommend for anyone diagonosed with sleep apnea and prescribed CPAP or BiPAP.

We found answers to some of the most critical questions about the ongoing recall of millions of CPAP machines, ventilators and other breathing devices.

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.