The following is a listing of U.S. Food and Drug Administration (FDA) updates and activities:

• Update: Certain Philips Respironics Ventilators, BiPAP Machines, and CPAP Machines Recalled Due to Potential Health Risks: FDA Safety Communication

• FDA Alerts Health Care Professionals of Compatibility Issues with Prefilled Glass Syringes and Certain Luer-Activated Valve (LAV) Connectors

• Update on Philips Respironics Recall: New Issues Identified in Reworked Trilogy Ventilators

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