Connected sleep devicemaker ResMed today released the AirSense 11, its latest CPAP machine iteration, which includes a host of new features to treat obstructive sleep apnea. The new machine has many ...

Please provide your email address to receive an email when new articles are posted on . ResMed CPAP masks that contain magnets are being recalled due to possible magnetic interference with medical ...

The U.S. Food and Drug Administration (FDA) on Thursday classified a product recall initiated by ResMed (NYSE:RMD) for its respiratory care devices, AirFit and AirTouch masks, as a Class I recall, the ...

A CPAP machine is a medical device often recommended to folks who have sleep apnea or other disruptive sleep conditions. Wearers place a mask over their nose and mouth to deliver a continuous stream ...

As Philips reaches a consent decree agreement with the FDA that will temporarily suspend its sales of sleep therapy devices in the U.S., competitor ResMed, meanwhile, is ramping up its product ...

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.

Add Yahoo as a preferred source to see more of our stories on Google. FILE PHOTO: Signage is seen outside of FDA headquarters in White Oak, Maryland (Reuters) - The U.S. Food and Drug Administration ...

ResMed may have clocked its highest-ever annual revenues in its 2023 fiscal year, but those gains seemingly weren’t enough to satisfy investors. In the days since the devicemaker reported its $4.2 ...

Amid a recall of its AirFit and AirTouch continuous positive airflow pressure (CPAP) devices, ResMed released its latest earnings report Wednesday afternoon. The San Diego-based medical device company ...

He distributed 440 reassembled devices, billing Medicaid over $600,000 for unclean, altered equipment.

If you've been following the Philips recall on certain respiratory devices, you might be wondering at this point if the recall will ever end. The answer to that question remains unclear, but the ...

Jan 11 (Reuters) - The U.S. Food and Drug Administration (FDA) on Thursday classified the recall of certain respiratory masks made by ResMed (RMD.N), opens new tab as most serious as their use could ...