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U.S. Department of Health and Human Services

Class 1 Device Recall Fire Star

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  Class 1 Device Recall Fire Star see related information
Date Initiated by Firm January 14, 2008
Date Posted February 06, 2008
Recall Status1 Terminated 3 on October 20, 2009
Recall Number Z-0814-2008
Recall Event ID 46378
PMA Number P880003 
Product Classification Dilatation Catheter - Product Code LOX
Product CORDIS "Fire Star" 3.00 x 20 Dilatation Catheter, Catalog # 80120300, Distributed by Cordis Corporation, Miami Lakes, FL 33014
Code Information Lot #s: 13187449 13191017 13197627 13200868 13212426 13212427 13218323 13224191 13226740 13230694 13231290 13233901 13239280 13246361 13247919 13252930 13281217 13281229 13281239 13281288 13281300 13281345 13281429 13281441 13281458 13282485 13283825 13286193 13290338 13294211 13294557 13294558 13301371 13303085 13304561 13311788 13311789 13311798 13312722 13314188 13321832 and  13325101 
Recalling Firm/
Manufacturer		 Cordis Corporation
14201 NW 60th Avenue
Miami Lakes FL 33014-2802
For Additional Information Contact
786-313-2000
Manufacturer Reason
for Recall		 Slow Deflation or No Deflation
FDA Determined
Cause 2		 Process control
Action Cordis initated the recall on 1/14/2008. For U.S. customers: An Urgent Medical Device Recall letter and an Acknowledgement Form was sent to the following 4 individuals in each account: Cath Lab Director, Operating Room Director, Materials Director, Risk Manager; to be followed up with direct Cordis representative contact to facilitate obtaining signature, faxing form, collecting and returning units. For non-US customers, email notification with return acknowledgement is used to notify the affiliate distributors, who then notify and reconcile the customers in those countries. All users were instructed to immediately set aside product and return it for replacement.
Quantity in Commerce 133,300 units total for recalls Z-0747-0824-2008
Distribution Worldwide.
Total Product Life Cycle TPLC 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.
PMA Database PMAs with Product Code = LOX and Original Applicant = CORDIS CORP.
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