Medical Device Recalls
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101 to 102 of 102 Results
510(K) Number: K081113 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Triple Lumen Polyurethane Catheter, ... | 1 | 02/23/2011 | Cook, Inc. |
Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Triple Lumen Polyurethane Catheter, ... | 1 | 02/23/2011 | Cook, Inc. |
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