Medical Device Recalls
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1 to 2 of 2 Results
Recall Date to: 05/24/2015 PMA Number: P020036 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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S.M.A.R.T. CONTROL NITINOL STENT SYSTEM ILIAC: Self-Expanding Vascular Stents delivered by catheter... | 2 | 02/15/2012 | Cordis Corporation |
CORDIS S.M.A.R.T.® Control" Nitinol Stent System Model Number(s): C10040SL, Manufactured in Mexico.... | 2 | 07/31/2008 | Cordis Corporation |
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