Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K791844 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| CRITIFLO(tm) FLUSH KIT | 2 | 10/21/2005 |
FEI # 1710034 Becton Dickinson Medical Systems |
| CRITIFLO(tm) TAK0460 continuous flow catheter | 2 | 10/21/2005 |
FEI # 1710034 Becton Dickinson Medical Systems |
| CRITIFLO(tm) flush kit. | 2 | 10/21/2005 |
FEI # 1710034 Becton Dickinson Medical Systems |
| CRITIFLOW(tm) TA4004 continuous flush catheter | 2 | 10/21/2005 |
FEI # 1710034 Becton Dickinson Medical Systems |
| DT-DL60-1 W/Bifurcated | 2 | 10/21/2005 |
FEI # 1710034 Becton Dickinson Medical Systems |
| DTX(tm) Plus DT-DL60 Continuous flush catheter | 2 | 10/21/2005 |
FEI # 1710034 Becton Dickinson Medical Systems |
| TAKHPQ60R continuous flow catheter. | 2 | 10/21/2005 |
FEI # 1710034 Becton Dickinson Medical Systems |
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