Product Safety Information
Ultraflex™ Esophageal and Ultraflex™ Tracheobronchial Stent Systems Recall
On May 17, 2010, Boston Scientific initiated a recall of specific lots of the Ultraflex™ Esophageal and Ultraflex™ Tracheobronchial Stent Systems.
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Liberté® Coronary Stent System
On September 18, 2009, Boston Scientific initiated a field correction for the Liberté® bare-metal (Liberté® Bare-Metal) coronary stent products.
Swiss LithoClast® Pneumatic Probes
On September 17th, 2009 Boston Scientific initiated a recall of specific lots of Swiss LithoClast® Pneumatic Probes.
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Coronary Catheter Recall
On August 5th, 2009, Boston Scientific initiated a recall removal of Wiseguide™ Guide Catheters, Impulse™ Angiographic Catheters, and Expo™ Angiographic Catheters.
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HTA® Procedure Set Recall
On July 31, Boston Scientific initiated a voluntary recall of all unexpired units of the HTA Procedure Set.
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Prolieve Thermodilatation® System Recall
On July 22, 2009, Boston Scientific initiated a voluntary recall of all unexpired units of the Prolieve Thermodilatation System Kit.
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