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

• Ventec Life Systems Recalls VOCSN Patient Breathing Package for Manufacturing Issue with Bonded Spiral Wrap

• Medtronic Duet External Drainage and Monitoring System Recalled Due to a Potential for Catheter Disconnection

• Baxter Healthcare ExactaMix Pro 1200 and Pro 2400 Recalled Due to a Software Error

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