Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K981660 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Percutaneous Insertion Tray; Product Code: IAK-S7IT The Arrow® IAB is utilized for intra aortic b... | 1 | 03/11/2016 |
FEI # 3010532612 Arrow International, Inc., Division of Teleflex Medical Inc. |
| RediGuard IAB: 7Fr 30cc; Product Code: IAB-S730C The Arrow® IAB is utilized for intra aortic ball... | 1 | 03/11/2016 |
FEI # 3010532612 Arrow International, Inc., Division of Teleflex Medical Inc. |
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