Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K062798 |
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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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Product is labeled in part: Inner Label "***SMART Control Transhepatic Biliary Stent***REF Cat. No.... | 2 | 05/10/2012 | Cordis Corporation |
Product is labeled in part: Inner Label "***S.M.A.R.T. Transhepatic Biliary Stent***REF Cat. No.***... | 2 | 05/10/2012 | Cordis Corporation |
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