FierceBiotech

ResMed tops $1B in Q2 revenues as Philips’ CPAP recall rages on

As Philips’ recall of many of its CPAP and BiPAP machines and other respiratory devices grew to include more machines and sparked tens of thousands of patient complaints, ResMed stepped up to fill ...
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 ...
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 ...
Seeking Alpha

ResMed product recall classified as most serious by FDA (update)

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 ...
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 ...
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.
Seeking Alpha

FDA issues safety warning over Philips DreamStation 2 CPAP machines

The FDA is warning patients and healthcare providers that it has received over 270 reports about Philips (NYSE:PHG) Respironics' DreamStation 2 CPAP machines overheating, which can lead to injury. In ...