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U.S. Department of Health and Human Services

Class 2 Device Recall Ultraflex tracheobronchial Stent System

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 Class 2 Device Recall Ultraflex tracheobronchial Stent Systemsee related information
Date Initiated by FirmMay 17, 2010
Date PostedJune 25, 2010
Recall Status1 Terminated 3 on October 20, 2011
Recall NumberZ-1823-2010
Recall Event ID 55784
510(K)NumberK012883 
Product Classification Prosthesis, tracheal, expandable - Product Code JCT
ProductUltraflex Tracheobronchial Stent System. Uncovered - 14/20 Catalog Number: M00568980. Single Use, Rx only. Boston Scientific, Natick, MA 01760. Indicated for the use in the treatment of tracheobronchial structures produced by malignant neoplasms.
Code Information Lot Numbers: 9790074 9790076 11003371 11003538 11059367 11118676 11118678 11187506 11187507 11242343 11242356 11270352 11296916 11296917 11377103 11377104 11433735 11434016 11470448 11487990 11488029 11514456 11514458 11554796 11554991 11610744 11639021 11639030 11677818 11678048 11757152 11757154 11793164 11793166 11837438 11837483 11876610 11876622 11979808 11979811 12025013 12025143 12054670 12054671 12066948   12066951 12092005 12147149 12147208 12163806 12163809 12184724 12184725 12185876 12185878 12269162 12269163 12277634 12277635 12545679 12600436 12621164 12702786 12723775 12740615 12830189 12935877 13165824 13187801 13207649 13230712  
Recalling Firm/
Manufacturer		 Boston Scientific Corporation
100 Boston Scientific Way
Marlborough MA 01752-1234
For Additional Information Contactsame
508-683-8000
Manufacturer Reason
for Recall		Suture related device failures during deployment and repositioning of the stent
FDA Determined
Cause 2		Device Design
ActionBoston Scientific issued an "Urgent Medical Device Recall - Immediate Action Required" notification dated May 17, 2010 to U.S. Distributors stating that use and distribution of products should cease immediately and return all affected product to the firm for replacement. Distributors were asked to complete and return reply a verification tracking form. For further information, contact Boston Scientific at 1-866-868-4004.
DistributionWorldwide Distribution - Only US distributed product is affected by recall
Total Product Life CycleTPLC Device Report
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.
510(K) Database510(K)s with Product Code = JCT
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