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 ...
The U.S. Food and Drug Administration has updated a recall affecting millions of Philips sleep apnea machines, now saying that they may been linked to at least 561 deaths. The agency, in a statement ...
Sleep apnea is a medical condition that affects an estimated 22 million Americans. Typical symptoms of sleep apnea include heavy snoring, excessive daytime sleepiness or fatigue, and difficulty with ...
Certain Philips Respironics DreamStation breathing devices, commonly used for treating sleep apnea, may deliver the incorrect prescription or no therapy at all, the FDA warned in a recall announcement ...
This is an archived article and the information in the article may be outdated.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. (WKBN) – More than 17 million masks for ...
The U.S. Food and Drug Administration is alerting patients, caregivers and health care providers that Philips Respironics has recalled certain BiPAP and CPAP masks due to a serious safety concern. The ...
Millions of people rely on machines to help them with sleep disorders, but now some of the devices have been recalled because they could pose serious health problems.The 11 News I-Team reported many ...
PHILADELPHIA, June 30, 2021 /PRNewswire/ — The national plaintiffs’ law firm Berger Montague has filed a class action lawsuit against Dutch medical equipment company Philips to protect consumers ...
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