Medical Device Recalls
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1 to 2 of 2 Results
Related Medical Device Recalls |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Z-0910-2013 - Leonard 10.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneous Introducer system (product code 0600630). Product Usage: Hickman and Leonard Catheters are ... | 2 | 03/06/2013 |
FEI # 3006260740 Bard Access Systems |
| Z-0909-2013 - Hickman 9.0 French Dual Lumen Catheter with SureCuff Tissue Ingrowth Cuff with Peel-Apart Percutaneous Introducer system (pediatric product code 0600580; adult product code 0600600). Product Usage:... | 2 | 03/06/2013 |
FEI # 3006260740 Bard Access Systems |
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