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.

More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration.

Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall ...

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 ...

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 ...

Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall FDA To determine if you have an affected model By CNN Newsource Published April 7, 2023 4:03 PM ...