Cordis Corporation Recall 88372
Description: Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
Cordis Corporation Recall 88372 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-2428-2021 |
| Event ID | 88372 |
| Event Description | Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB |
| Product Type | Devices |
| Distribution | Worldwide distribution - US Nationwide distribution and the countries of Canada, Europe. |
| Quantity | 45 units |
| Recall Reason | Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Marker Bands) are being used in a manner that may allow entrapment of the catheter between endovascular devices and the vessel wall, which can lead to marker band movement or dislodgement. |
| Device Classification | 20210922 |
| Device Code Info | All codes |
| Center Classification Date | 20210915 |
| Recall Initiation Date | 20210721 |
| Recalling Firm | Cordis Corporation |
| Initial Notification | Letter |
| Similar To |