Cordis Corporation: 17 recalls on record

Recalls filed with 1 agency: FDA (17).

First recall on record: October 3, 2012. Most recent: November 24, 2021.

Risk classification: Class I: 1 · Class II: 15 · Class III: 1

Most recent recalls

DateAgencyProduct
November 24, 2021FDASMART FLEX 6x150 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for u…Z-0218-2022
April 24, 2019FDACordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding cathete…Z-1198-2019
November 14, 2018FDACordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate steno…Z-0390-2019
September 3, 2014FDACordis EMPIRA RX PTCA Dilatation CatheterZ-2557-2014
September 3, 2014FDACordis EMPIRA NC RX PTCA Dilatation CatheterZ-2556-2014
June 18, 2014FDACordis EMPIRA RX PTCA Dilatation Catheter Catalog # 85R30300S For cardiovascular use.Z-1784-2014
November 6, 2013FDACordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pu…Z-0081-2014
October 9, 2013FDACordis ADROIT 6F Guiding Catheter Product Usage: For intravascular introduction of in…Z-0003-2014
August 14, 2013FDACordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat. No.***466F220A and 46…Z-1887-2013
June 12, 2013FDAFLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The FSS FLEXST…Z-1508-2013
June 12, 2013FDAFLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The FSS FLEXST…Z-1511-2013
June 12, 2013FDAFLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The FSS FLEXST…Z-1510-2013
June 12, 2013FDAFLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Bili…Z-1509-2013
June 12, 2013FDAFLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Bili…Z-1507-2013
February 6, 2013FDACordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat. No…Z-0740-2013
October 3, 2012FDASleek ***OTW ***Ref ***426-1501X***Inflated Balloon Dia/mm 1.5 Inflated Balloon Length/mm…Z-2442-2012
October 3, 2012FDASleek OTW***REF 426-1201X***Inflated Balloon Dia/mm***1.25***Inflated Balloon Length/mm**…Z-2441-2012

Questions about this company

How many recalls does Cordis Corporation have?
Recalert has 17 U.S. recalls on record for Cordis Corporation, published between October 3, 2012 and November 24, 2021.
What was the most recent Cordis Corporation recall?
FDA recall Z-0218-2022, published November 24, 2021: SMART FLEX 6x150 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the biliary tree.
Which agencies have handled Cordis Corporation recalls?
Cordis Corporation appears as the recalling firm in recalls from: FDA (17).

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