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 ...
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, ...
Almost two full years into its Class I recall of more than 5 million respiratory devices, Philips has wrapped up safety tests covering nearly all of the affected models—and is reiterating its previous ...
PHILADELPHIA, June 30, 2021 /PRNewswire/ — The national plaintiffs’ law firm Berger Montague has filed a class action lawsuit against Dutch medical equipment company Philips to protect consumers ...
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 ...
Due to a shortage of lifesaving breathing machines amid the COVID-19 (coronavirus) pandemic, the U.S. Food and Drug Administration (FDA) issued guidelines last month that allow hospitals, universities ...
This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. California Gov. Gavin Newsom responded ...
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