The Food and Drug Administration on Thursday classified the voluntary recall of certain respiratory masks made by ResMed as “most serious” as their incorrect use could cause major injuries or death.

Millions of masks used with sleep apnea machines have been recalled for safety concerns. Philips Respironics recalled more than 17 million masks used with their continuous positive airway pressure or ...

Please provide your email address to receive an email when new articles are posted on . Several clinical and CPAP-related variables were linked to a greater risk for high residual apnea-hypopnea index ...

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 ...

Please provide your email address to receive an email when new articles are posted on . The FDA has granted de novo clearance to SoClean 3+, an over-the-counter bacterial reduction device for certain ...