The company also added that the recall doesn’t affect Philips’ ongoing efforts to repair and replace all of the CPAP and BiPAP machines and other ventilators included in the initial 2021 recall.

A maker of machines for sleep apnea patients has agreed to a $479 million settlement related to a recall of its devices ... positive airway pressure, or CPAP, machines, CBS News reported.

the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has determined a reasonable probability that a product could “cause ...

According to Philips, the recall of millions of CPAP breathing machines was due to "potential risks" that included "toxic and carcinogenic effects," along with the possibility of developing ...

6, the FDA announced several of the masks used with bilevel positive airway pressure (also known as Bilevel PAP, BiPAP or BPAP) machines and continuous positive airway pressure (CPAP) machines ...

It took more than a decade after users first reported the soundproofing foam in their CPAP and BPAP machines breaking down for Philips to issue a recall. Even after the recall notice was issued ...

The IntelliPAP AutoAdjust can be used in both conventional CPAP or AutoAdjust modes. The system allows clinicians to adjust the apnea and hypopnea detection to the individual standards.

An online reviewer is warning about a CPAP machine recall. He claims The Philips Dreamstation CPAP device, recalled in 2023, is still being used and could pose a cancer risk to users. Uncle Nicko ...

The IntelliPAP Standard is the first CPAP in the IntelliPAP range. It is a fixed pressure device ranging from 3 cm H2O to 20 cm H2O. The DeVilbiss IntelliPAP Standard CPAP System was designed with ...