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 ...
CNN — 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 ...
PHILLIPS HAS NOW RECALLED ALMOST 20 DIFFERENT MODELS OF CPAP AND BIPAP MACHISNE BECSEAU OF HEALTH CONCERNS. THE COMPANY SAYS THAT THE PHONE THAT IS INSIDE OFHE T MACHINES TO DAMPEN THE SOUND CAN BREAK ...
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 ...
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