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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K830233
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FDA Recall
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Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneo... 2 03/06/2013 FEI # 3006260740
Bard Access Systems
Leonard 10.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutane... 2 03/06/2013 FEI # 3006260740
Bard Access Systems
Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Tissue Ingrowth Cuff Cat 60060 ... 2 02/13/2026 FEI # 2020394
Bard Peripheral Vascular Inc
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