SAN DIEGO, Sept. 30, 2024 (GLOBE NEWSWIRE) -- ResMed (NYSE: RMD, ASX: RMD), the world’s leading health technology company focused on sleep, breathing, and care delivered in the home, today announced a ...

SAN DIEGO - ResMed, two years after Respironics rocked the CPAP world with the debut of its wildly popular C-Flex device, has finally answered the challenge with a similar form of therapy, called EPR.

Sleep apnea, a widespread sleep disorder manifested as breathing cessation episodes during sleep, is experienced by a lot of people. Being subject, such a problem prompts deterioration of life quality ...

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 ...

ResMed is a major player in the PAP market. Credit: sbw18 via Shutterstock. ResMed’s Class I recall of its AirFit and AirTouch continuous positive airflow pressure (CPAP) masks threatens the company’s ...

The AirTouch N20, one of the devices affected by the corrective action. [Image from ResMed] The FDA announced that ResMed’s voluntary recall of millions of CPAP mask magnets is now Class I, the agency ...

ResMed Chief Product Officer Justin Leong and Global Sleep Product Manager Lai Ying Ho discuss the AirFit F40 mask’s design and development. If you search FDA records for ResMed’s new AirFit F40 ...

As the global supply chain has begun to slowly untangle itself over the past few months, ResMed has finally been able to scale up production of its sleep apnea hardware and start to fill the massive ...

Magnets in continuous positive airway pressure (CPAP) masks led to Class I recalls in recent years for Philips Respironics and ResMed. Those recalls — classified as the most serious kind by the FDA ...

ResMed’s voluntary recall of some of its CPAP mask magnets has now been labeled as Class I by FDA. The agency announced the classification late last week. In November, ResMed began recalling some ...