Zenith Alpha Spiral-Z Endovascular Leg, Catalog Prefix ZISL. The product is an endovascular graft.
Recall
- Recall Number
- Z-1355-2020
- Event Number
- 84778
- Firm
- Cook Inc.
- FEI Number
- 1820334
- Product Code
- MIH
- Status
- Terminated
- Root Cause
- Labeling design
- Initiated
- January 16, 2020
- Posted
- January 31, 2020
- Terminated
- November 12, 2020
- Address
- 750 N Daniels Way, Bloomington, IN, 47404-9120
Description
Zenith Alpha Spiral-Z Endovascular Leg, Catalog Prefix ZISL. The product is an endovascular graft.
The firm has identified factors which contributed to failures relating to thrombus formation and/or lumen occlusion reports, and is highlighting to customers key points of the IFU pertaining to the prevention of these factors. In addition, the firm has updated the Planning and Sizing Worksheet to include associated information.
On January 14, 2020, the firm notified affected customers via Urgent Medical Device Correction letters/emails. Customers were advised to pay especial attention to several aspects of the Instructions for Use (IFU) which were of key importance when implanting a device. Customers were also provided with an updated Planning and Sizing Worksheet. If you have any questions or concerns, please contact Cook Medical Customer Relations at 800.457.4500 or 812.339.2235.
Foreign distribution only. Distributed worldwide.
68,241