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 ...

The Food and Drug Administration issued a new warning for users of certain CPAP machines – the latest in a series of troubles for Philips Respironics, one of the leading manufacturers of the breathing ...

SALISBURY, Md. - There was a recall on more than 3 million Philips Respironics CPAP and BiPAP machines. These devices are used to treat patients who suffer from sleep apnea. According to a statement ...

The manufacturer, Philips Respironics, said it would compensate users of CPAP machines and other flawed devices that were recalled after they blew bits of foam into consumers’ mouths and lungs. By ...

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Almost two full years into its Class I recall of more than 5 million respiratory devices, Philips has wrapped up safety tests covering nearly all of the affected models—and is reiterating its previous ...

Lake Charles, LA (KPLC) - Millions of masks used with sleep apnea machines have been recalled for safety concerns. Philips Respironics has recalled over 17 million of its masks used with their CPAP ...

In June of 2021, Philips Respironics issued a recall for some of its CPAP and BiPAP machines. Now the U.S. Food and Drug Administration says the notification to users about the recall “have been ...

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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 ...

Royal Philips Electronics and Cinterion Wireless Modules, the global leader in cellular machine-to-machine (M2M) communication modules, announced recently that the Philips Respironics System One sleep ...