Medical Device Recalls
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1 result found
510(K) Number: K112636 |
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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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| CytoGuard Closed Luer Connector, Intravenous access 2 cartons of 50 units each (100 units per case) | 2 | 05/23/2017 |
FEI # 3003218564 B Braun Medical Inc |
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