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 ...

Investor group European Investors-VEB on Wednesday applied for a court inquiry into Philips over allegations of misleading ...

Sept 8 (Reuters) - Paris prosecutors opened a criminal probe into Philips (PHG.AS), opens new tab in June over its recall of sleep apnea devices, probing possible charges including aggravated fraud ...

(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 ...

The Food and Drug Administration yesterday announced that Olympus issued a global recall of its ViziShot 2 FLEX needles ...