CORDIS "Fire Star" 2.00 x 10, Dual Marker Band, Dilatation Catheter, Catalog # 8011020D, Distributed by Cordis Corporation, Miami Lakes, FL 33014
FDA Recall Z-0789-2008 · Posted 2008-02-06
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Recalling FirmCordis Corporation
Recall StatusTerminated
Product CodeLOX
Date Initiated2008-01-14
Date Terminated2009-10-20
Product Quantity133,300 units total for recalls Z-0747-0824-2008
Reason for Recall
Slow Deflation or No Deflation
Firm 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.
Root Cause
Process control
Distribution Pattern
Worldwide.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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