Product Safety Information
Boston Scientific IMAGER™ II Catheter Recall
On March 15, 2012, Boston Scientific Corporation initiated a Medical Device Recall of certain lots/batches of the IMAGER™ II Catheter.
Peripheral Intervention Customer Letter »
Peripheral Intervention Affected Product List »
Urology Customer Letter and Affected Product List »
Urgent Notification: Potential Risk of Infection
Boston Scientific devices were recently stolen prior to being sterilized. The stolen shipment affects certain Endoscopy and Urology/Women’s Health devices shipped between April 8, 2011 and April 11, 2011.
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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.
Download customer notice and product listings
Customer Notice »
Esophageal Product Listing »
Tracheobronchial Product Listing »
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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