Medical Device Recalls
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21 to 22 of 22 Results
510(K) Number: K862056 |
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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| Arrow Multi-Lumen CVC w/ BlueFlex Tip (Central Venous Catheter) | 2 | 06/24/2009 |
FEI # 3015859709 Arrow International Inc |
| Arrow central venous catheterization kit, 14 ga x 20 cm | 3 | 11/01/2003 |
FEI # 3015859709 Arrow International Inc |
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