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

ResMed warns against using magnetic CPAP masks around pacemakers, other implants

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 ...
FierceBiotech

ResMed’s warning on CPAP magnet interference earns FDA Class I recall tag

In late November, ResMed issued a safety notice warning that some of the masks used with its CPAP machines contain magnets that could potentially interfere with pacemakers, neurostimulators and other ...
Seeking Alpha

ResMed issues urgent safety notice over magnetic CPAP masks

ResMed (NYSE:RMD) has issued an urgent safety notice for masks used with continuous positive airway pressure, or CPAP, machines over concerns that magnets contained in the masks may interfere with ...
Nasdaq

ResMed Notifies Customers About Updated Instructions and Labeling for Masks with Magnets Due to Potential Interference with Certain Medical Devices

SAN DIEGO, Dec. 20, 2023 (GLOBE NEWSWIRE) -- ResMed (NYSE: RMD, ASX: RMD) is conducting a voluntary global field action to update its guides for all masks with magnets to inform users about potential ...
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.
Nasdaq

ResMed says its masks to remain on market despite FDA classification

Jan 16 (Reuters) - ResMed said its respiratory masks containing magnets will remain on the market even though the U.S. Food and Drug Administration classified a recall of the product as most serious ...