Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K830755 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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15 Drop IV Sets, with Retractable Luer-Lock and with Smartsite(TM) Y-Injection sites and 4-Way Stopc... | 1 | 03/30/2010 | Arrow International Inc |
10 Drop IV Sets, with 3 Pre-Pierced Y-Injection Sites and 3-Gang Pressure Activated Manifold Valve. ... | 1 | 03/30/2010 | Arrow International Inc |
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