Medical Device Recalls
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21 to 25 of 25 Results
510(K) Number: K000729 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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8 Fr 40cc Ultra 8 IAB, IAB-05840-U, Intra-aortic balloon catheter. The Intra-aortic balloon (IAB... | 1 | 04/16/2009 | Arrow International, Inc. |
8 Fr 30cc Ultra 8 IAB, IAB-05830-U, Intra-aortic balloon catheter. The Intra-aortic balloon (IAB... | 1 | 04/16/2009 | Arrow International, Inc. |
8 Fr 40cc Narrow Flex IAB Catheter Kit with Generic Adapters Product Number: IAB-04840-U, Intra-aor... | 1 | 04/16/2009 | Arrow International, Inc. |
ARROW 50cc Drive Line Kits, REF IAK-02693, Intra-aortic balloon catheter. The Intra-aortic ball... | 1 | 04/16/2009 | Arrow International, Inc. |
8 Fr 30cc Narrow Flex IAB Catheter Kit with Generica Adapters Product Number: IAB-04830-U, Intra-ao... | 1 | 04/16/2009 | Arrow International, Inc. |
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