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U.S. Department of Health and Human Services

Medical Device Recalls
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121 to 123 of 123 Results
Related Medical Device Recalls Recall Date to: 07/03/2015
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Product Description
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FDA Recall
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Z-1216-2011 - Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Triple Lumen Polyurethane Catheter, 9 Fr/ 20 cm, C-UTLMY-901J-RSC-ABRM-HC-FST-A-RD, G51587, Sterile, Cook Medical, Cook Incorporated, B... 1 02/23/2011 Cook, Inc.
Z-1217-2011 - Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Triple Lumen Polyurethane Catheter, 9 Fr/ 25 cm, C-UTLMY-901J-LSC-ABRM-HC-FST-A-RD, G51588, Sterile, Cook Medical, Cook Incorporated, B... 1 02/23/2011 Cook, Inc.
Z-1218-2011 - Spectrum Central Venous Tray Minocycline/Rifampin Impregnated Triple Lumen Polyurethane Catheter, 9 Fr/ 20 cm, C-UTLMY-901J-RSC-ABRM-HC-IHI-FST-A-RD, G51590, Sterile, Cook Medical, Cook Incorporate... 1 02/23/2011 Cook, Inc.
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