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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 of 80 Results
Recall Date to: 03/06/2015 PMA Number: P880003
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Product Description
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FDA Recall
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CORDIS "Dura Star" 2.75 x 20 Dilatation Catheter, Catalog # 70120275, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.00 x 20 Dilatation Catheter, Catalog # 70120300, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.25 x 20 Dilatation Catheter, Catalog # 70120325, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.50 x 20 Dilatation Catheter, Catalog # 70120350, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.75 x 20 Dilatation Catheter, Catalog # 70120375, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 4.00 x 20 Dilatation Catheter, Catalog # 70120400, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.25 x 25 Dilatation Catheter, Catalog # 70125225, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.50 x 25 Dilatation Catheter, Catalog # 70125250, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 2.75 x 25 Dilatation Catheter, Catalog # 70125275, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
CORDIS "Dura Star" 3.00 x 25 Dilatation Catheter, Catalog # 70125300, Distributed by Cordis Corporat... 1 02/06/2008 Cordis Corporation
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