Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-0790-2011 - Arrow Ultra 8 IAB (Intra-Aortic Balloon) Catheter, 8 Fr, 30cc. Model: IAB-05830-U | 1 | 12/23/2010 | Arrow International, Inc., Division of Teleflex Medical Inc. |
| Z-0791-2011 - Arrow Ultra 8 IAB (Intra-Aortic Balloon) Catheter, 8 Fr, 40cc. Model: IAB-05840-U | 1 | 12/23/2010 | Arrow International, Inc., Division of Teleflex Medical Inc. |
| Z-0969-2011 - Percutaneous Insertion Tray For Use with: Arrow Ultra 8 IAB (Intra Aortic Balloon) Catheters Model: IAK-05845 | 1 | 12/23/2010 | Arrow International, Inc., Division of Teleflex Medical Inc. |
| Z-0793-2011 - FiberOptix IAB Ultra 8 Fr, 40cc Model: IAB-05840-LWS | 1 | 12/23/2010 | Arrow International, Inc., Division of Teleflex Medical Inc. |
| Z-0792-2011 - FiberOptix IAB Sheath, Ultra 8 Fr, 30cc. Model: IAB-05830-LWS | 1 | 12/23/2010 | Arrow International, Inc., Division of Teleflex Medical Inc. |
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