Medical Device Recalls
-
1 to 6 of 6 Results
PMA Number: P180029 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, ... | 1 | 01/09/2021 | Boston Scientific Corporation |
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 23mm, ... | 1 | 01/09/2021 | Boston Scientific Corporation |
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 25mm, ... | 1 | 01/09/2021 | Boston Scientific Corporation |
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 25mm, ... | 1 | 01/09/2021 | Boston Scientific Corporation |
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 27mm, ... | 1 | 01/09/2021 | Boston Scientific Corporation |
Lotus Edge Valve System, Transcatheter Aortic Valve Prosthesis Premounted on Delivery System, 27mm, ... | 1 | 01/09/2021 | Boston Scientific Corporation |
-