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U.S. Department of Health and Human Services

Medical Device Recalls

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61 to 70 of 102 Results
510(K) Number: K081113
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Product Description
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FDA Recall
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Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Double Lumen Polyurethane With Mini... 1 02/23/2011 Cook, Inc.
Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated 5 Lumen Polyurethane, 10.0 Fr/ 15... 1 02/23/2011 Cook, Inc.
Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated 5 Lumen Polyurethane, 10.0 Fr/ 15... 1 02/23/2011 Cook, Inc.
Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Triple Lumen Polyurethane, 5.0 Fr... 1 02/23/2011 Cook, Inc.
Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Triple Lumen Polyurethane, 5.0 Fr... 1 02/23/2011 Cook, Inc.
Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Five Lumen Polyurethane, 5.0 Fr/ ... 1 02/23/2011 Cook, Inc.
Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Triple Lumen Polyurethane, 5.0 Fr... 1 02/23/2011 Cook, Inc.
Spectrum Central Venous Tray, Minocycline/Rifampin Impregnated Triple Lumen Polyurethane, 5.0 Fr... 1 02/23/2011 Cook, Inc.
Central Venous Tray, Triple Lumen Polyurethane, 9.0 Fr/ 15cm, C-UTLMY-901J-CCT-RD, G48997, Steril... 1 02/23/2011 Cook, Inc.
Central Venous Catheter Tray, Triple Lumen Polyurethane, 9.0 Fr/ 25cm, C-UTLMY-901J-LSC-CCT-RD, G... 1 02/23/2011 Cook, Inc.
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