If you or a loved one have been injured or suffered a loss due to a defective Intra-Aortic Balloon Pump Catheter you may be entitled to compensation. Conatact the IAB Pump Catheter Attorneys of Ennis & Ennis, P.A. today for a free case evaluation by filling out the online form on this page or call toll free: 1-800-856-6405. Our experienced IAB Pump Catheter Lawyers can answer any questions you may have about the Arrow Catheter Recall and potential IAB Pump Catheter Lawsuit.

Arrow Intra-Aortic Balloon Pump Catheter Recall - IAB Catheter Lawyer - IAB Catheter Recall Lawsuit - Balloon Catheter Attorney

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Arrow International Announces Worldwide Voluntary Recall Of Intra Aortic Balloon Pump (IAB) Catheters|
-Medical News Today
04/16/2009 - Teleflex Medical announced today that the U.S. Food and Drug Administration (FDA) has classified the voluntary medical device recall initiated on February 2, 2009 by Arrow International's Cardiac Care Division involving volume connectors for its 30cc, 40cc and 50cc Intra Aortic Balloon Pump (IAB) Catheters as a Class 1 recall. More>>>

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