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 charges including aggravated fraud and failure to report safety incidents that ...

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

NEW YORK (AP) — Ford is recalling more than 355,000 of its pickup trucks across the U.S. because of an instrument panel display failure that's resulted in critical information, like warning lights and ...

The Food and Drug Administration (FDA) said Southwind Foods, LLC, is voluntarily recalling a range of frozen shrimp products that may be contaminated with cesium-137, a man-made radioactive isotope ...