Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K970864 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Arrow Three-Lumen CVC | 2 | 06/27/2022 | ARROW INTERNATIONAL Inc. |
12 French 3 Lumen 20 cm Large-Bore Central Venous Catheters. Product numbers AK-15123-H, AK-15123-J... | 2 | 08/10/2009 | Arrow International Inc |
12 French 3 Lumen 16 cm Large-Bore Central Venous Catheters. Product numbers AK-12123-H, CS-12123-E... | 2 | 08/10/2009 | Arrow International Inc |
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