Medical Device Recalls
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61 to 63 of 63 Results
510(K) Number: K002507 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Radial Artery Catheterization Kit with Sharps Safety Features The Arrow® Arterial Catheterization d... | 2 | 06/06/2017 | Arrow International Inc |
Two-Lumen Hemodialysis Catheterization Kit with Blue Flex Tip(R), ARROWg+ard Blue(R) Catheter, Sharp... | 2 | 06/06/2017 | Arrow International Inc |
Two-Lumen Hemodialysis Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue(R) Catheter, Sharps... | 2 | 06/06/2017 | Arrow International Inc |
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