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ResMed was recalling some models of its continuous positive airway pressure (CPAP) masks, AirFit and AirTouch, due to possible magnetic interference with certain medical devices and implants which ...
The FDA defines a recall as a method of removing or correcting products that are in violation of laws administered by the health regulator and does not include a market withdrawal. ResMed's masks ...
CPAP and BiPAP machines are both worn at night to help those with sleep apnea. Last week, the U.S. Food and Drug Administration (FDA) announced that previously recalled sleep apnea machines have ...
Even switching to a different model can be precarious. Halting recalled CPAP or BiPAP machines can also be "unacceptably risky" for certain patients, physicians warned in the American Journal of ...
A 2021 recall of Philips breathing devices is related to 561 deaths, the U.S. Food and Drug Administration said Wednesday. 561 deaths linked to recalled Philips sleep apnea machines, FDA says Skip ...
The company behind a global recall of sleep apnea machines said Monday it will stop selling the devices in the U.S., under a tentative agreement with regulators that could cost the manufacturer ...
Earlier this year, Dutch medical device maker Royal Philips reached a $1.1 billion deal to settle thousands of claims stemming from a recall in 2021 of millions of its breathing machines like ...
The recall in the U.S. covers certain Chevrolet Silverado and GMC Sierra 1500, 2500, and 3500 pickups from the 2020 through 2022 model years. Also included are the 2021 Cadillac Escalade, GMC ...
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