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

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

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

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.

Philips is actively engaged with policymakers in Washington about investigations into U.S. imports of medical technology ...

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