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

VEB has applied to the Enterprise Chamber of the Amsterdam Court of Appeal, claiming that Philips' failing information ...

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.

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

LOS ANGELES (KABC) -- Rather than weight loss and surgery, getting a CPAP machine has been the top go-to treatment for people with a severe snoring disorder called sleep apnea. But after the Food and ...

(Reuters) - Paris prosecutors opened a criminal probe into Philips in June over its recall of sleep apnea devices, probing possible charges including aggravated fraud and failure to report safety ...

Technology company Philips plans to cut an estimated 5% of its workforce, about 4,000 positions, due to losses caused by the recall of a sleep apnea product as well as supply chain issues, according ...

Philadelphia, PA – The CPAP lawsuit, which has drawn national attention, is focused on CPAP, BiPAP, and ventilator devices, which are alleged to have produced potentially carcinogenic particles.