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.

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

The prosecutor’s office opened an investigation in June, with charges including aggravated fraud and failure to report incidents that pose serious health risks.

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

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 ...

Airway Management proudly announces a historic milestone with the FDA clearance of Nylon flexTAP ® , the world’s first digitally printed single-point midline oral appliance device for sleep apnea.

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

Philips and Masimo are renewing their yearslong collaboration in patient monitoring with what they describe as an expanded ...

In patients with both type 2 diabetes and obstructive sleep apnea, treatment with CPAP may reduce the risk for mortality.

The multi-year agreement comes two months after Philips renewed a partnership for patient monitoring technologies with Masimo ...

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