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July 16, 2021

FDA Safety Communication

The U.S. Food and Drug Administration (FDA) is alerting people who use Philips Respironics ventilators, BiPAP, and CPAP machines and their health care providers that Philips Respironics has recalled certain devices (see table below) due to potential health risks.

Don't forget to keep your family's information up-to-date in DEERS.