Medical Device Recalls
-
1 to 5 of 5 Results
Related Medical Device Recalls |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
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. |
-