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

• Arrow International, LLC, a Subsidiary of Teleflex, IncRecalls Arrow AutoCAT 2, AC3 Intra-Aortic Balloon Pumps for Unexpectedly Short Battery Run Times

• Teleflex and Arrow International, LLC Recall Arrow MAC Two-Lumen Central Venous Access and Pressure Injectable Arrowg+ard Blue Plus Three-Lumen Central Venous Catheter (CVC) Kits

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