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

In partnership with Pittsburgh Post-Gazette. The massive recall of DreamStation machines and other breathing devices disrupted medical care for millions in the United States and around the world.

The Food and Drug Administration says 561 deaths have been reported in connection to recalled Philips devices to treat obstructive sleep apnea and other breathing disorders. The FDA said that since ...

Earlier this week, the U.S. Department of Justice, representing the Food and Drug Administration and healthcare technology company Philips came to an agreement to no longer sell their sleep therapy or ...

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