Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K820648 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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4Fr. Catheter Clamp with Fastener; Product Code: CC-00004 | 2 | 05/30/2018 | Arrow International Inc |
7Fr. Catheter Clamp with Fastener; Product Code: CC-00007 | 2 | 05/30/2018 | Arrow International Inc |
5Fr. Catheter Clamp with Fastener; Product Code: CC-00005 | 2 | 05/30/2018 | Arrow International Inc |
8Fr. Catheter Clamp with Fastener; Product Code: CC-00008 | 2 | 05/30/2018 | Arrow International Inc |
Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter, ARROW g+ard Blue Catheter | 2 | 09/25/2010 | Arrow International Inc |
Multi-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features) | 2 | 09/25/2010 | Arrow International Inc |
Two-Lumen Central Venous Catheterization kit with Blue FlexTip Catheter (Sharps Safety Features) | 2 | 09/25/2010 | Arrow International Inc |
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