BiPAP and CPAP masks help people with obstructive sleep apnea, respiratory insufficiency or respiratory failure — health conditions that cause pauses in breathing during sleep.

More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration.

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 ...

The recall stems from Philips’ finding that the magnets embedded in some of its CPAP and BiPAP masks may interact with certain implanted medical devices in both the wearers of the masks and ...

More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration.

More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration.

The latest of these came to light this week when both Philips and the FDA alerted users of its CPAP and BiPAP machines—and their caregivers and healthcare providers—to a potential health risk ...

BiPAP and CPAP masks help people with obstructive sleep apnea, respiratory insufficiency or respiratory failure — health conditions that cause pauses in breathing during sleep.

17M Philips CPAP, BiPAP masks recalled over ‘serious safety concern’ The FDA said a “serious safety concern” with magnets prompted the recall.

More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration.

17M Philips CPAP, BiPAP masks recalled over ‘serious safety concern’ The FDA said a “serious safety concern” with magnets prompted the recall.