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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Percutaneous Insertion Tray; Product Code: IAK-06845 The Arrow® IAB is utilized for intra aortic ... | 1 | 03/11/2016 | Arrow International, Inc., Division of Teleflex Medical Inc. |
Ultra 8 IAB: 8Fr 30cc; Product Code: IAB-05830-U The Arrow® IAB is utilized for intra aortic ball... | 1 | 03/11/2016 | Arrow International, Inc., Division of Teleflex Medical Inc. |
Ultra 8 IAB: 8Fr 40cc; Product Code: IAB-05840-U The Arrow® IAB is utilized for intra aortic ball... | 1 | 03/11/2016 | Arrow International, Inc., Division of Teleflex Medical Inc. |
UltraFlex IAB: 7.5Fr 30cc; Product Code: IAB-06830-U The Arrow® IAB is utilized for intra aortic ... | 1 | 03/11/2016 | Arrow International, Inc., Division of Teleflex Medical Inc. |
UltraFlex IAB: 7.5Fr 40cc; Product Code: IAB-06840-U The Arrow® IAB is utilized for intra aortic ... | 1 | 03/11/2016 | Arrow International, Inc., Division of Teleflex Medical Inc. |
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