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 July 1, 2019, a new law took effect in Georgia that mandates that patients with dense breast tissue identified on their mammograms be notified of this finding in the letter they receive explaining their mammogram results.