Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.

Philips Respironics has removed certain DreamStation devices due to programming errors that can result in failed therapy modes, according to the U.S. Food and Drug Administration.

Earlier this week, the U.S. Department of Justice, representing the Food and Drug Administration and healthcare technology company Philips came to an agreement to no longer sell their sleep therapy or ...

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 ...