Dutch medical device maker Philips said Monday it had reached a $1.1 billion deal in the United States to settle lawsuits over faulty sleep machines in a case that have dogged the company. The company ...
WASHINGTON — A device made by Philips Respironics for treating sleep apnea should be monitored closely when in use because it can overheat, according to federal regulators. The Food and Drug ...
The FDA is warning patients and healthcare providers that it has received over 270 reports about Philips (NYSE:PHG) Respironics' DreamStation 2 CPAP machines overheating, which can lead to injury. In ...
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 ...
Nov 28 (Reuters) - Philips (PHG.AS), opens new tab shares fell more than 6% on Wednesday after the U.S. Food and Drug Administration said, opens new tab it is alerting patients of a new safety issue ...
Please provide your email address to receive an email when new articles are posted on . Reports of fire, smoke, burns and other signs of overheating are emerging for DreamStation 2 CPAP machines by ...
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 ...
SILVER SPRING, Md., Nov. 28, 2023 /PRNewswire/ -- Today, as part of the U.S. Food and Drug Administration's continued commitment to protect and promote the public health, the agency is alerting ...
The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...
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