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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 50 of 80 Results
Recall Date to: 12/18/2014 PMA Number: P880003
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Product Description
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FDA Recall
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CORDIS "Dura Star" 3.75 x 30 Dilatation Catheter, Catalog # 70130375, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 4.00 x 30 Dilatation Catheter, Catalog # 70130400, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Fire Star" 1.50 x 10, Dual Maker Band, Dilatation Catheter, Catalog # 8011015D, Distributed ... 1 02/06/2008 Cordis Corporation
CORDIS "Fire Star" 1.50 x 10, Single Marker Band, Dilatation Catheter, Catalog # 8011015S, Distribut... 1 02/06/2008 Cordis Corporation
CORDIS "Fire Star" 2.00 x 10, Dual Marker Band, Dilatation Catheter, Catalog # 8011020D, Distributed... 1 02/06/2008 Cordis Corporation
CORDIS "Fire Star" 2.00 x 10, Single Marker Band, Dilatation Catheter, Catalog # 8011020S, Distribu... 1 02/06/2008 Cordis Corporation
CORDIS "Fire Star" 2.25 x 10 Dilatation Catheter, Catalog # 80110225, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Fire Star" 2.50 x 10 Dilatation Catheter, Catalog # 80110250, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Fire Star" 2.75 x 10 Dilatation Catheter, Catalog # 80110275, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Fire Star" 3.00 x 10 Dilatation Catheter, Catalog # 80110300, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
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