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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 80 Results
PMA Number: P880003
 
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Product Description
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FDA Recall
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CORDIS "Dura Star" 2.25 x 10 Dilatation Catheter, Catalog # 70110225, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.50 x 10 Dilatation Catheter, Catalog # 70110250, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.75 x 10 Dilatation Catheter, Catalog # :70110275, Distributed by Cordis Corpora... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.00 x 10 Dilatation Catheter, Catalog # 70110300, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.25 x 10 Dilatation Catheter, Catalog # 70110325, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.50 x 10 Dilatation Catheter, Catalog # 70110350, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.75 x 10 Dilatation Catheter, Catalog # 70110375, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 4.00 x 10 Dilatation Catheter, Catalog # 70110400, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.25 x 15 Dilatation Catheter, Catalog # 70115225, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.50 x 15 Dilatation Catheter, Catalog # 70115250, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
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