An initial report Philips issued in early September said the recall affected “more than 17 million” of certain masks used with CPAP and BiPAP machines, but the FDA now counts a total of 18,670,643 ...

Magnets embedded in many of Philips’ masks used with CPAP and BiPAP machines could potentially interfere with implanted medical devices, including pacemakers, neurostimulators, metallic stents, ocular ...

WASHINGTON - Philips Respironics has recalled more than 17 million masks used for people with sleep apnea and other respiratory issues due to a safety issue with magnets that could affect certain ...

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 ...

The Food and Drug Administration (FDA) has issued a safety communication regarding the recall of certain Philips Respironics masks used with bilevel positive airway pressure (also known as Bi-Level ...

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 ...

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 ...

Add Yahoo as a preferred source to see more of our stories on Google. The FDA said a “serious safety concern” with magnets prompted the recall. Super Bowl 2026: Seahawks OC Klint Kubiak confirms ...