Medical Device Recalls
-
1 to 4 of 4 Results
510(K) Number: K943934 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Sorin Group Aortic Arch Cannula, 7 mm x 10 in x 3/8 in, Rx Only, Sterile Product Usage: The Aort... | 2 | 08/10/2017 | Sorin Group USA, Inc. |
Aortic Arch Cannula and Coronary Artery Perfusion Cannula with Ballon (part number NA-55X6). The Aor... | 2 | 09/08/2016 | Sorin Group USA, Inc. |
AORTIC ARCH CANNULA, Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass (part numbers NA... | 2 | 07/08/2016 | Sorin Group USA, Inc. |
Dual Stage Venous Return Catheter, Low-Profile, wire reinforced (36F/46F, Sterile), Model Number: LR... | 2 | 02/16/2016 | Sorin Group USA, Inc. |
-