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

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

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

Roy Jakobs, who joined Philips in 2010 and became CEO in 2022 amid a major crisis, has since played a key role in stabilizing the company.

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.

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 ...

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 ...

Paris prosecutors have launched a criminal investigation into Philips over its 2021 recall of sleep apnea devices. The probe ...

The global Wearable Healthcare Devices Market, valued at US$41.07 billion in 2024, stood at US$45.29 billion in 2025 and is ...

Despite media reports suggesting a fresh investigation, France has not initiated a new probe into Philips' recall of sleep ...

France has not opened a new investigation into the recall of Philips' sleep apnea devices, a spokesperson for the company ...