OKLAHOMA CITY (KFOR) – The U.S. Food and Drug Administration (FDA) is urging CPAP and other ventilator users to check their machines over a deadly recall. Since April 2021, the FDA has received 561 ...

Decree Includes Key Provisions Aimed to Prioritize Patient Relief and Ensure Company's Regulatory Compliance "The finalization of this decree is a significant milestone. Throughout this recall, we ...

The Food and Drug Administration said 561 deaths are reportedly tied to recalled sleep apnea devices made by Philips Respironics. This comes as Philips Respironics this week agreed to stop selling new ...

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 ...

Medical device maker Phillips formally entered into a consent decree that stops the company from selling sleep apnea machines in the United States over health concerns that include cancer. The decree ...

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Technology company Philips plans to cut an estimated 5% of its workforce, about 4,000 positions, due to losses caused by the recall of a sleep apnea product as well as supply chain issues, according ...

SILVER SPRING, Md., April 9, 2024 /PRNewswire/ -- Today, the U.S. District Court for the Western District of Pennsylvania entered a consent decree of permanent injunction against Philips RS North ...