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

• Embolization Device Recall and Correction: Medtronic Removes Unused 027 Compatible Pipeline Vantage Embolization Device with Shield Technology, Updates Use Instructions for 021 Compatible Pipeline Vantage Embolization Devices due to Increased Risk of Incomplete Wall Apposition and Braid Deformation

• Implantable Port Recall: Smiths Medical Removes ProPort Plastic Implantable Ports Due…

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