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BiPAP vs. CPAP: What’s the Difference?

Continuous positive airway pressure (CPAP) and BiPAP (bi-level) therapy are used to treat sleep apnea. CPAP is the most ...
The FDA announced that recalled CPAP and BiPAP machines have been tied to hundreds of deaths. The CPAP and BiPAP machines were initially recalled in June 2021. CPAP and BiPAP machines are both worn at ...
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 ...
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 ...
WASHINGTON — Medical equipment company Philips Respironics has recalled at least 17 million masks used with breathing devices designed to treat patients with sleep apnea and other respiratory ...
This is an archived article and the information in the article may be outdated.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 ...
BATON ROUGE, La. (WAFB) - The U.S. Food and Drug Administration is alerting patients, caregivers and healthcare providers Philips Respironics (Philips) recalled certain masks due to a safety concern.
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 ...