AMSTERDAM, NETHERLANDS (WTEN0) – Philips Respironics has issued a recall on thousands of ventilators and CPAP machines. The recall only affects units sold in the United States. The units affected ...

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

LOS ANGELES (KABC) -- Rather than weight loss and surgery, getting a CPAP machine has been the top go-to treatment for people with a severe snoring disorder called sleep apnea. But after the Food and ...

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.

Medical device company Philips announced a recall of millions of sleep apnea machines and ventilators because a material used inside them could put users at risk of cancer or other health issues.

Paris prosecutors opened a criminal probe into Philips in June over its recall of sleep apnea devices, probing possible ...

Philips sent updated instructions related to a problem with bilevel positive airway pressure, or BiPAP, machines that can cause interruption or loss of therapy. Philips recalled three models of BiPAP ...