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 ...
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 ...
Philips has recalled more than 17 million CPAP and BiPAP masks because the product’s magnets can interfere with implanted metal medical devices, such as pacemakers. As of Sept. 6, there have been 14 ...
There is a risk of serious injury or death related to more than 20 million CPAP masks made by ResMed, the FDA said Jan. 11. The continuous positive airway pressure masks, branded as AirFit and ...
There is major medical recall involving machines many people use to sleep every night.The U.S. Food and Drug Administration announced Tuesday night they are recalling Phillips BiPAP and CPAP masks ...
Some sleep therapy masks made by Philips Respironics present a potential risk of serious injury for people with pacemakers or other metallic implants. Jessica was a writer on the Wellness team, with a ...
This is an archived article and the information in the article may be outdated.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 trouble seemingly never ends for Philips’ beleaguered Respironics division. Since beginning a recall of around 5.5 million ventilators and other breathing support machines more than a year ago, in ...
As competitor Philips continues to grapple with the effects of its long-standing recall of continuous positive airway pressure (CPAP) machines and other respiratory devices, ResMed is now issuing a ...
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