Cordis Corporation CORDIS "Dura Star" 3.50 x 20 Dilatation Catheter, Catalog # 70120350, 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" 3.50 x 20 Dilatation Catheter, Catalog # 70120350, 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 13173918 13180565 13183028 13195992 13200886 13211073 13260774 13264256 13266341 13267183 13270375 13272420 13273243 13280399 13280400 13282481 13284565 13302232 13303064 13306831 and 13313282
Cordis Corporation is recalling CORDIS "Dura Star" 3.50 x 20 Dilatation Catheter, Catalog # 70120350, 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