The U.S. Food and Drug Administration (FDA) is alerting people who use Philips Respironics ventilators, BiPAP, and CPAP machines and their health care providers that Philips Respironics has recalled ...
(KAKE/FDA) - Philips Respironics has voluntarily recalled certain ventilators, BiPAP, and CPAP machines due to potential health risks. The polyester-based polyurethane (PE-PUR) sound abatement foam, ...
Magnets in the recalled masks, used in breathing machines for sleep apnea, can interfere with pacemakers and other lifesaving medical devices. Philips Respironics has voluntarily recalled more than 17 ...
Philips Respironics has recalled some face masks used with CPAP and BiPap machines because they have magnetic headgear clips that can interfere with other medical devices. The recalled masks are the ...
Millions of people across the country were jostled awake this year over fearful news: A critical device they were prescribed and relied on each night for sleep was suddenly labeled a hazard to their ...
A North Texan, navigating the recall of some CPAP and BiPAP machines made by Philips Respironics, learned the company says it’s too old to repair. Read on for how she found a resolution. For years, ...
Philips, after a year and a half of discussions with the Department of Justice (DOJ) on behalf of FDA, today announced the company and FDA has agreed to a consent decree related to the 2021 ...
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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