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 ...
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 ...
Philips Respironics is recalling millions of CPAP, BiPAP and ventilators due to potential health risks related to polyester-based polyurethane sound abatement foam. It’s been just over a year since ...
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 ...
Just a few weeks after racking up its fifth Class I recall from the FDA this year, Philips has hit the half-dozen mark. Its sixth of the classifications—which denote the agency’s most serious rating ...
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 ...
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