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 ...
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 ...
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 ...
Philips Respironics announced last Monday that it’s stopping sales of their breathing machines within the U.S. following a mid-2021 product recall. The decision, as reported by The New York Times, was ...
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 ...
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 ...
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 ...
Murraysville, Pa.-based Philips Respironics has issued a worldwide recall of its Trilogy Ventilators Models 100, 200 and 202 due to a potentially faulty component on the ventilators’ power boards. The ...
This article originally appeared on 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.
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 ...
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