CORPUS CHRISTI, Texas — As the number of COVID-19 cases in our country rise, supplies are dwindling. Medical professionals facing a shortage of ventilators in some areas of the country are turning to ...
CORPUS CHRISTI, Texas — If you have a CPAP or BiPAP machine that you no longer need there is a way to put it to good use during the COVID-19 pandemic. CPAP and BiPAP machines are generally used by ...
As the coronavirus pandemic rips through the U.S., governors have made public pleas for more personal protective equipment (PPE) for health care and frontline workers, and for ventilators to help ...
Get all the latest news on coronavirus and more delivered daily to your inbox. Sign up here. As doctors face a shortage of ventilators that are crucial for treating coronavirus patients with ...
(WKBN) – More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration. The FDA said that Philips Respironics (Philips) has recalled ...
The U.S. Food and Drug Administration is alerting patients, caregivers and health care providers that Philips Respironics has recalled certain BiPAP and CPAP masks due to a serious safety concern. The ...
Certain Philips Respironics ventilators, BiPAP, CPAP machines recalled due to potential health risks
(News release) - The U.S. Food and Drug Administration (FDA) is alerting people who use Philips Respironics ventilators, BiPAP, and CPAP machines and their health care providers that Philips ...
In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...
The trouble seemingly never ends for Philips’ beleaguered Respironics division. Since beginning a recall of around 5.5 million ventilators and other breathing support machines more than a year ago, in ...
The U.S. Food and Drug Administration has updated a recall affecting millions of Philips sleep apnea machines, now saying that they may been linked to at least 561 deaths. The agency, in a statement ...
The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...
Millions of people rely on machines to help them with sleep disorders, but now some of the devices have been recalled because they could pose serious health problems.The 11 News I-Team reported many ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results
Feedback