Philips sent updated instructions related to a problem with bilevel positive airway pressure, or BiPAP, machines that can cause interruption or loss of therapy. Philips recalled three models of BiPAP ...
A custom-made valve fits to the top of full-face masks, where the snorkel is meant to go, allowing them to connect to standard BiPAP machines that feed pressurised air into masks AFP / Kenzo ...
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 ...
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 ...
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 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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