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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 12 Results
510(K) Number: K980290
 
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Product Description
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Recall
Class
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FDA Recall
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ev3 IntraStent Biliary Stent, Model Number: S10-26, ev3, 4600 Nathan Lane North, Plymouth, MN 5544... 2 05/06/2008 Ev3, Inc
ev3 IntraStent DoubleStrut Biliary Stent, Model Number: S11-16, ev3, 4600 Nathan Lane North, Plym... 2 05/06/2008 Ev3, Inc
ev3 IntraStent DoubleStrut Biliary Stent, Model Number: S11-26, ev3, 4600 Nathan Lane North, Plym... 2 05/06/2008 Ev3, Inc
ev3 IntraStent DoubleStrut Biliary Stent, Model Number: S11-36, ev3, 4600 Nathan Lane North, Plym... 2 05/06/2008 Ev3, Inc
ev3 IntraStent LD DoubleStrut Large Diameter Biliary Stent, Model Number: S15-16, ev3, 4600 Nath... 2 05/06/2008 Ev3, Inc
ev3 IntraStent LD Max Large Diameter Biliary Stent, Model Number: S18-36, ev3, 4600 Nathan Lane N... 2 05/06/2008 Ev3, Inc
ev3 IntraStent LD Mega Large Diameter Biliary Stent, Model Number: S17-16, ev3, 4600 Nathan Lane ... 2 05/06/2008 Ev3, Inc
ev3 IntraStent LD Mega Large Diameter Biliary Stent, Model Number: S17-26, ev3, 4600 Nathan Lane ... 2 05/06/2008 Ev3, Inc
ev3 IntraStent LD Mega Large Diameter Biliary Stent, Model Number: S17-36, ev3, 4600 Nathan Lane ... 2 05/06/2008 Ev3, Inc
ev3 IntraStent LD Max Large Diameter Biliary Stent, Model Number: S18-16, ev3, 4600 Nathan Lane N... 2 05/06/2008 Ev3, Inc
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