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 ...
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 ...
Philips Respironics is recalling some of its BiPAP machines due to a plastic that can contaminate the machine and cause it to fail, according to the U.S. Food and Drug Administration (FDA). The ...
Philips Respironics recalled more than 17 million masks used with their continuous positive airway pressure, or CPAP, and bilevel positive airway pressure, or BIPAP machines. The Food and Drug ...
NEW HYDE PARK, N.Y.--(BUSINESS WIRE)--In preparation for potential patient surge and shortage of critical mechanical ventilators for hospitalized COVID-19 patients, a Northwell Health physician, a ...