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.

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 affected items, ranging from kitchen appliances to child safety products, pose hazards including burns and strangulation.

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

FDA expands BD Alaris Pump Module 8100 recall, adding 15 infusion sets due to serious health risks. Read more here.