If you use a Philips CPAP machine, you have another thing to keep you awake at night: The FDA issued a warning Tuesday to patients and health care providers saying the company’s DreamStation 2 ...

People who have bought, leased or rented certain Philips Respironics sleep apnea machines can now file a claim for restitution. The Dutch medical equipment maker recently agreed to pay at least $479 ...

In 2021, polyester-based polyurethane (PE-PUR) foam used in Philips Respironics ventilators, CPAP and BiPAP machines was found to degrade and cause serious health issues or death, leading to a mass ...

STATEN ISLAND, N.Y. — The U.S. Food and Drug Administration (FDA) is urging caution when using a certain Philips CPAP machine, due to possible safety issues. The agency is alerting patients and health ...

Millions of CPAP sleep apnea machines made by the medical device maker Philips and a subsidiary were found to have a dangerous problem, triggering consumer lawsuits and a massive recall in 2021. Now, ...

This article originally appeared in ProPublica. ProPublica is a Pulitzer Prize-winning investigative newsroom. Sign up for The Big Story newsletter to receive stories like this one in your inbox. For ...

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 ...

Three years after one of the largest medical device recalls in history, the fallout – health-wise and financial – continues to impact many patients with sleep apnea. Now a critical deadline is ...

AND HAS THE NEW INFORMATION TONIGHT. THE OWNERS OF PHILIPS RESPIRONICS, CPAP AND OTHER BREATHING MACHINES ARE RECEIVING THIS NOTICE IN THE MAIL OF A PROPOSED CLASS ACTION SETTLEMENT. EIGHT ON YOUR ...

Philips DreamStation 2 continuous positive airway pressure (CPAP) machines should be monitored for signs of overheating, according to the Food and Drug Administration (FDA). The Philips DreamStation 2 ...

In a Nov. 28 safety alert, the FDA warned patients and healthcare providers to carefully monitor Philips machines used for obstructive sleep apnea after receiving reports that the machines have shown ...