Cordis Corporation CORDIS "Dura Star" 2.50 x 15 Dilatation Catheter, Catalog # 70115250, Distributed by Cordis Corporation, Miami Lakes, FL 33014 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
CORDIS "Dura Star" 2.50 x 15 Dilatation Catheter, Catalog # 70115250, Distributed by Cordis Corporation, Miami Lakes, FL 33014
Brand
Cordis Corporation
Lot Codes / Batch Numbers
Not specified in FDA notice. Check official source for details.
Products Sold
Lot #s: 13175337 13180560 13183023 13195487 13195988 13207209 13209762 13209915 13209925 13211070 13216629 13217623 13222115 13250079 13250082 13255236 13255238 13271057 13275168 13277834 13278672 13285156 13290329 13291123 13298189 13298786 13300595 13303780 13305487 13310112 and 13314812
Cordis Corporation is recalling CORDIS "Dura Star" 2.50 x 15 Dilatation Catheter, Catalog # 70115250, Distributed by Cordis Corporat due to Slow Deflation or No Deflation. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Slow Deflation or No Deflation
Recommended Action
Per FDA guidance
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.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026