RecallDepth

Zenith Alpha Spiral-Z Endovascular Leg, Catalog Prefix ZISL. The product is an endovascular graft.

Company
Cook, Inc.
Recall Initiated
January 16, 2020
Posted
January 31, 2020
Terminated
November 12, 2020
Recall Number
Z-1355-2020
Quantity
68,241
Firm Location
Bloomington, IN

Reason for Recall

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.

Distribution

Foreign distribution only. Distributed worldwide.

Lot / Code Info

All lots. OUS distribution only; Product is not cleared or distributed in the USA.

Root Cause

Labeling design

Action Taken

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.

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