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U.S. Department of Health and Human Services

Medical Device Recalls
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141 to 150 of 500 Results *
Recall Date to: 06/29/2015
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Product Description
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Recall
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FDA Recall
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ev3, Prot®g® Rx Tapered Carotid Stent System, SEPX-8-6-40-135, Sterile EO, Rx only. Indicated fo... 2 12/29/2014 Ev3, Inc.
ev3" 55442-2920, sterile EO, single Use, Visi-Pro Balloon-Expandable Peripheral Stent System. Mode... 2 09/26/2008 Ev3, Inc
ev3" sterile EO, single Use, Visi-Pro Balloon-Expandable Biliary Stent System. Model Numbers: P... 2 09/26/2008 Ev3, Inc
ev3 The Endovascular Company, Protege GPS 8mm x 40mm Self Expanding Peripheral Stent System , Rx Onl... 2 09/08/2009 Ev3, Inc.
ev3 The Endovascular Company, Protege GPS 8mm x 40mm Self Expanding Biliary Stent System, Rx Only, a... 2 09/08/2009 Ev3, Inc.
ev3 The Endovascular Company, Protege GPS 6mm x 80mm Self Expanding Peripheral Stent System , Rx On... 2 09/08/2009 Ev3, Inc.
ev3 The Endovascular Company, Protege GPS 6mm x 80mm Self Expanding Biliary Stent System, Rx Only, a... 2 09/08/2009 Ev3, Inc.
ev3 The Endovascular Company, IntraCoil Self-Expanding Peripheral Stent, Model REF VT-6-60-135, Lot ... 3 09/21/2008 Ev3, Inc
ev3 Prot®g® EverFlex Self-Expanding Biliary Stent System, Sterile EO, (REF: PRB35-06-150-080, REF P... 2 05/13/2010 Ev3, Inc.
ev3 Protege Rx Tapered Carotid Stent System, SECX-10-7-40-135, Sterile EO, Rx only. Indicated fo... 2 12/29/2014 Ev3, Inc.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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