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Home » FDA Issues Update on Philips Respironics Mask Recall
FDA Issues Update on Philips Respironics Mask Recall
The FDA has provided an update on Philips Respironics’ recall of almost 18.7 million masks for use with bilevel positive airway pressure (BiPAP) and continuous positive airway pressure (CPAP) machines, deeming the recall Class 1 because of the risk of serious injury or death.