Philips CPAP and BiPap machines that were recalled in 2021 have since been linked to deaths and thousands of malfunctions, the FDA says ...

Pulmonology > Sleep Disorders Reworked Philips CPAP, BiPAP Machines May Not Deliver Correct Therapy — And some of the remediated breathing devices may not provide any treatment at all, FDA warns ...

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 agency, in a statement issued last week, said it has received more than 116,000 reports about the breathing devices — BiPAP and CPAP machines — over nearly three years.

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.

Philips released the latest set of safety test results (PDF) on Tuesday, covering all of the CPAP and BiPAP sleep therapy machines included in the recall—which together make up about 95% of all ...

The agency, in a statement issued last week, said it has received more than 116,000 reports about the breathing devices — BiPAP and CPAP machines — over nearly three years.

The agency, in a statement issued last week, said it has received more than 116,000 reports about the breathing devices — BiPAP and CPAP machines — over nearly three years.

The agency, in a statement issued last week, said it has received more than 116,000 reports about the breathing devices — BiPAP and CPAP machines — over nearly three years.