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 ...

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.

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 ...