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 ...

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 ...

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 ...

ResMed (NYSE:RMD) intends to keep its CPAP masks that utilize magnets on the market despite a recall because it regards the action as a labeling correction rather than a product removal. According to ...

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 ...

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.

Air Voel Expands Product Line with the Latest ResMed CPAP Machines for Enhanced Sleep Therapy. Canada - November 8, 2024 — Air Voel, a leading provider of CPAP solutions in Canada, is proud to ...