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Home » Philips Respironics Ordered to Notify Patients of Breathing Assistance Machine Recall
Philips Respironics Ordered to Notify Patients of Breathing Assistance Machine Recall
In a rare move by the FDA, the agency ordered Philips Respironics to notify patients and other customers of the company’s June 14, 2021, recall of certain models of its ventilators, continuous positive airway pressure (CPAP) and bilevel positive-airway pressure (BiPAP) machines.