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 ...

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

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 ...