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.

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

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.

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