Times of San Diego

FDA: Voluntary Recall of CPAP Masks by San Diego’s ResMed Addresses ‘Serious’ Problem

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.
MD&M East

ResMed's CPAP Warning Is Now a Class I Recall

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 ...
Healio

ResMed CPAP masks subject to Class I recall over magnetic interference issue

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 ...
FierceBiotech

FDA clears Resmed AI for personalizing CPAP settings

The goal is to streamline setup and reduce the manual adjustments needed at the start of CPAP therapy, when people are still tinkering with the mask fit and other issues. (ResMed) Resmed believes its ...