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Class 2 Device Recall |
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Date Initiated by Firm |
June 10, 2004 |
Date Posted |
July 27, 2004 |
Recall Status1 |
Terminated 3 on November 01, 2004 |
Recall Number |
Z-1205-04 |
Recall Event ID |
29300 |
PMA Number |
P020018 |
Product Classification |
System, Endovascular Graft, Aortic Aneurysm Treatment - Product Code MIH
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Product |
Cook brand Zenith AAA Iliac leg graft with the H&L-B One-Shot Introducer System, preloaded iliac leg graft - distal cuff diameter 22 mm - usable length 54mm - delivery system 16 FR; Catalog no. TFLE-22-54. |
Code Information |
Lots F1564212, F1564213, F1573033, F1573034, F1573035, F1573036, F1573037, F1564266, F1564267, F1564268, F1564269, F1566711, F1566712, F1569316, F1564422, F1564423, F1564424 and F1564425. |
Recalling Firm/ Manufacturer |
Cook, Inc. 750 Daniels Way Bloomington IN 47404-9120
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For Additional Information Contact |
Customer Relations 800-457-4500
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Manufacturer Reason for Recall |
Introducer tubing may contain a vein of unextruded material and carbon black or a strand of tubing material may be displaced from the introducer during use.
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FDA Determined Cause 2 |
Other |
Action |
The firm issued recall letters to customers on 6/10/04. The recall was extended and URGENT EXTENSION OF PRODUCT RECALL notices were sent out on June 23, 2004. |
Quantity in Commerce |
18 |
Distribution |
Nationwide, Canada, Denmark and Japan. |
Total Product Life Cycle |
TPLC Device Report
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1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
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PMA Database |
PMAs with Product Code = MIH and Original Applicant = COOK, INC.
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