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.

Snoring and sleep apnea are issues that affect thousands of people across Hawai‘i, and while CPAP machines are often ...

According to a 2024 peer-reviewed clinical trial published in the European Respiratory Journal, Back2Sleep demonstrated a 64% ...

LONDON, GREATER LONDON, UNITED KINGDOM, September 11, 2025 /EINPresswire.com/ -- What Is The Home Sleep Apnea Testing Devices Market Size And Growth? The market size of home sleep apnea testing ...

Nyxoah announced today that it filed a lawsuit against Inspire Medical Systems alleging the infringement of sleep apnea therapy patents.

Stability is great, but low-volatility stocks may struggle to deliver market-beating returns over time as they sometimes ...

The research highlights an unsettling link between nighttime oxygen loss and long-term cognitive health. The team behind the ...

Here are four of the latest recalls and corrections reported to the FDA.

Paris prosecutors opened a criminal probe into Philips in June over its recall of sleep apnea devices, probing possible ...

When people first hear about portable power stations, their immediate question is not about technical specifications but about real-world usefulness. Can this device keep my food cold during a ...

James Collins, a 29-year-old hospital administrator from Travis, couldn’t understand what was causing his chronic fatigue.