The recall affects three million to four million machines, more than half of which are in the U.S., a company spokesman said Monday. About 80% are machines for aiding people with sleep apnea ...

Philips is recalling breathing devices and ventilators due to foam that might degrade and become toxic, possibly causing cancer, the Dutch medical equipment maker said on Monday. The recall ...

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 ...

Foam used to dampen the machines' sound can degrade and emit small particles that irritate airways, the group said as it announced the recall. Gases released by the degrading foam may also be ...

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 ...

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.

Philips on Monday announced that it will recall several ventilators and CPAP breathing machines after it discovered that a small foam component in the machines might degrade and be inhaled ...

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 ...