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 recall affects hair dryers sold under the Remington brand, model number D3190DCDN, which lack an immersion protection device, the Consumer Product Safety Commission announced. The recalled hair ...

More Than 55,000 Popular Hair Dryers Are Being Recalled For This Serious Reason originally appeared on Parade. A popular hair dryer brand is recalling one of its models due to "risk of serious injury ...

The FDA has issued a notice warning of a device correction related to ventilators from Philips Respironics. This marks the latest recall development for the Respironics business at the Dutch medtech ...

Javascript must be enabled to use this site. Please enable Javascript in your browser and try again. Learn how food choices can nurture your brain health Help ...

La Pine resident Bill Minnix initiated the recall petition against Kotek for what he claims are violations of her oath of office and for her support of undocumented immigrants. Minnix and his group, ...

MODESTO, Calif. (AP) — Energy drinks that mistakenly contain vodka are being recalled in half a dozen states. High Noon is recalling two production lots of High Noon Beach Variety packs because some ...