Philips' CPAP and BiPAP mask recall stretches to 22M devices, ... should immediately stop using the masks and ask their doctors if an alternative mask could be used for their CPAP or BiPAP therapy.

Philips Respironics has voluntarily recalled more than 17 million sleep apnea masks with magnetic parts that can cause implanted medical devices with metal parts to malfunction — including ...

Recall alert: 17M Philips CPAP, BiPAP masks recalled over ‘serious safety concern’ By Michelle Ewing, Cox Media Group National Content Desk September 08, 2022 at 7:11 am EDT ...

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 FDA said a “serious safety concern” with magnets prompted the recall.

Philips said that as of Aug. 30, it has received 14 reports linking implant malfunctions to the mask magnets. The incidents include issues with the devices, like pacemaker interference and failure ...

The mask recall was announced after 14 serious injuries were reported, including pacemaker failure, arrhythmia, seizures, and irregular blood pressure, the FDA said.

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 ...

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 conditions ...

Philips recalls masks for BiPAP, CPAP machines The U.S. Food and Drug Administration is warning patients, caregivers and healthcare providers that Philips Respironics (Philips) recalled certain ...

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 conditions ...

SILVER SPRING, Md., Sept. 6, 2022 /PRNewswire/ -- Today, the U.S. Food and Drug Administration is alerting patients, caregivers and health care providers that Philips Respironics (Philips) has ...