睡眠時無呼吸症候群のCPAP(持続陽圧呼吸)療法で用いられるフィリップスの人工呼吸器に、内部のポリウレタンフォームが剥離して装置使用者が吸い込んだり飲み込んだりする不具合があることがわかりました。フィリップスは数百万台を対象としてリコール ...

FROM SHADYSIDE TONIGHT. PHILIPS REIS RUN ROAD RECALLED MILLIONS OF CPAPS BIPAPS AND VENTILATORS AFTER THE FDA SAID FOAM INSULATION INSIDE THOSE MACHINES WAS A HEALTH RISK. BUT IN A LAWSUIT, PHILIPS ...

UPDATE (2024-07-05): Update on Philips Respironics recall of several models of CPAP and BiLevel PAP machines and mechanical ventilators Once consumers have completed the registration process, they ...

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 ...

Medical device maker Philips announced a nearly $1.1 billion personal injury settlement over some of its CPAP, ventilators and BiPAP machines that were at the heart of a massive recall in 2021. The ...

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 ...

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 company Philips reached a settlement Monday to shell out $1.1 billion to cover hundreds of personal injury lawsuits linked to its respiration and sleep apnea machines. The manufacturer ...

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 ...