Teleflex Incorporated Announces Worldwide Recall of ARROW International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits - FDA Safety Alerts & Drug Recalls

Teleflex Incorporated announces worldwide recall of ARROW International Intra-Aortic Balloon Catheter Kits and Percutaneous Insertion Kits. The Arrow IAB is inserted in the aorta and provides mechanical circulatory support for cardiac patients, by inflating and deflating at different phases of the cardiac cycle to increase cardiac output and decrease the work of the heart.

from Food and Drug Administration--Recalls/Safety Alerts http://ift.tt/1MbQ2kZ
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