Philips Respironics issued an Urgent Medical Device Correction notice for certain magnetic face and nasal masks due to potential health risks related to interaction between the magnets used in the masks and certain implanted medical devices. To learn more, please click on the links below:
For questions about this medical device correction, please contact Philips at 1-800-345-6443.
Philips Respironics issued a Recall Notification for some CPAP and BiLevel PAP devices and mechanical ventilators due to potential health risks related to foam used in the devices. To learn more, visit the Philips Website and review FDA’s Safety Communication and FAQs. For questions about the Philips recall, please contact Philips at 1-877-907-7508.
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