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Class 2 Device Recall Cook Urological Endoureterotomy Stent Set |
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Date Initiated by Firm |
July 31, 2008 |
Date Posted |
January 23, 2009 |
Recall Status1 |
Terminated 3 on November 27, 2009 |
Recall Number |
Z-0842-2009 |
Recall Event ID |
48760 |
510(K)Number |
K961446
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Product Classification |
Stent - Product Code FAD
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Product |
Cook Urological Endoureterotomy Stent Set, 10Fr/13 cm, 6.0Fr/24 cm, sterile, Cook Urological, Inc., Spencer, IN; Ref EUSCFS-060024-10-13; GPN REF G18132. Ureteral stent. |
Code Information |
Lots U1528861, U1542982, U1402436, U1361233, U1551529, U1391927, U1364946, U1347423, U1328716, U1416939, U1356437, U1525569, U1391927, U1328716, U1377093 and U1532644. |
Recalling Firm/ Manufacturer |
Vance Products Incorporated 1100 W Morgan St Spencer IN 47460-9426
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For Additional Information Contact |
812-339-2235 Ext. 7241
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Manufacturer Reason for Recall |
The bond may break where the two materials meet, resulting in separation of the stent.
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FDA Determined Cause 2 |
Process control |
Action |
Consignees were notified via "Urgent: Recall Notice" letter dated 7/31/08. The letter described the failure, instructed that the products be isolated and returned to the firm. For additional information, contact Cook Urological at 1-812-339-2235, ext. 7241. |
Quantity in Commerce |
1739 of all products. |
Distribution |
Nationwide, Australia, Canada, Colombia, Hong Kong, India, Ireland, Israel, Japan, Malaysia, Mexico, South Korea, Taiwan, Venezuela and Viet Nam |
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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510(K) Database |
510(K)s with Product Code = FAD and Original Applicant = COOK UROLOGICAL, INC.
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