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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 10 Results
510(K) Number: K920755
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Recall
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FDA Recall
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BD L-Cath EX (28ga x 20cm), L-Cath Catheter System 2 07/20/2004 Becton Dickinson Infusion Therapy
BD L-Cath EX (20ga x 15cm), L-Cath Catheter System 2 07/20/2004 Becton Dickinson Infusion Therapy
BD L-Cath NN (24ga x 30cm), L-Cath Catheter System 2 07/20/2004 Becton Dickinson Infusion Therapy
16 G / 5F Dual Lumen L-Cath Basic Kit with Introsyte 2 12/15/2005 Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Complete Kit with Introsyte 2 12/15/2005 Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Basic Kit with U-Wing 2 12/15/2005 Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Complete Kit with Introsyte Autoguard 2 12/15/2005 Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath complete kit with U-Wing 2 12/15/2005 Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath catheter only. 2 12/15/2005 Becton Dickinson Medical Systems
16 G / 5F Dual Lumen L-Cath Basic Kit with Insyte Autoguard 2 12/15/2005 Becton Dickinson Medical Systems
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