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 ...
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 ...
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 ...
STAT

How the CPAP crisis has paved the way for Philips’ biggest rivals to rake in profits

The Philips respiratory machine recall is a no-win situation for patients and doctors. But for the medical device giant’s longtime rivals and new competitors, business is looking up. “We think it will ...
FierceBiotech

ResMed launches new bi-level sleep apnea device as CPAP alternative

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 ...