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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Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes | 2 | 09/30/2015 | Arrow International Inc |
MAC Two-Lumen Central Venous Access kit with Integral Hemostasis Valve for use with 7 - 8 Fr. Cathet... | 2 | 09/25/2010 | Arrow International Inc |
Arrow Two-Lumen Central Venous Access (MAC) | 2 | 06/24/2009 | Arrow International Inc |
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