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.

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 ...

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

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