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.

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.

The patent-pending invention provides an improved face mask for use with a Bi-level Positive Airway Pressure (BiPAP) machine. In doing so, it would evacuate body fluids from within the mask.

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.

Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall By Jen Christensen and Katherine Dillinger, CNN Apr 7, 2023 1 of 2 ...