Philips Respironics Recall Notice:
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.
On June 14, 2021 Phillips issued a recall on CPAP and BiPAP devices manufactured between 2009 and April 2021. If your device is recalled or if you are not sure, you need to do the following:
COVID-19 Vaccine Information
Northside has started administering vaccines to physicians and staff. Please visit the Centers for Disease Control and Prevention for more information about the vaccine and the rollout to the community. Visit the Centers for Disease Control and Prevention.