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U.S. Department of Health and Human Services

Medical Device Recalls

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31 to 40 of 80 Results
Recall Date to: 10/25/2014 PMA Number: P880003
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Product Description
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FDA Recall
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CORDIS "Dura Star" 3.25 x 25 Dilatation Catheter, Catalog # 70125325, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.50 x 25 Dilatation Catheter, Catalog # 70125350, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.75 x 25 Dilatation Catheter, Catalog # 70125375, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 4.00 x 25 Dilatation Catheter, Catalog # 70125400, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.25 x 30 Dilatation Catheter, Catalog # 70130225, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.50 x 30 Dilatation Catheter, Catalog # 70130250, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.75 x 30 Dilatation Catheter, Catalog # 70130275, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.00 x 30 Dilatation Catheter, Catalog # 70130300, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.25 x 30 Dilatation Catheter, Catalog # 70130325, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.50 x 30 Dilatation Catheter, Catalog # 70130350, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
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