Philips (NYSE:PHG) has issued corrections for some of its Trilogy Evo ventilator platforms due to multiple issues.

ProSomnus announced today that it received FDA 510(k) clearance for its RPMO₂ obstructive sleep apnea (OSA) therapy device.

Add Yahoo as a preferred source to see more of our stories on Google. A doctor in Washington was sentenced to a year in jail for a scheme involving recalled Philips CPAP machines and ventilators. Both ...

A doctor in Washington was sentenced to a year in jail for a scheme involving recalled Philips CPAP machines and ventilators. Both support life; CPAPs help people with sleep apnea, which can lead to ...

Philips Respironics has updated use instructions for three bi-level positive airway pressure machines, according to a recall statement posted by the US FDA. The recall does not include removal of the ...

An online reviewer is warning about a CPAP machine recall. He claims The Philips Dreamstation CPAP device, recalled in 2023, is still being used and could pose a cancer risk to users. Featured Video ...

The settlement, which resolves claims by more than 4 million class members, does not provide monetary relief and includes more than $4.8 million in attorney fees and costs. In 2021, Philips recalled ...

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 ...

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. Teresa Murray, a consumer watchdog with the ...

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 ...

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