Cordis recalls
Cordis appears in 39 official U.S. recall notices indexed by RecallRadar, most recently on 2021-11-24.
Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.
- SMART FLEX 6x120 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the…
FDA Device · Class II · 2021-11-24 · Cordis - 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…
FDA Device · Class II · 2021-11-24 · Cordis - SMART FLEX 10x100 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in th…
FDA Device · Class II · 2021-11-24 · Cordis - SMART FLEX 10x100 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the…
FDA Device · Class II · 2021-11-24 · Cordis - SMART FLEX 8x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the b…
FDA Device · Class II · 2021-11-24 · Cordis - SMART FLEX 9x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant strictures in the b…
FDA Device · Class II · 2021-11-24 · Cordis - Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
FDA Device · Class I · 2021-09-22 · Cordis - Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB
FDA Device · Class I · 2021-09-22 · Cordis - Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B
FDA Device · Class I · 2021-09-22 · Cordis - Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598A
FDA Device · Class I · 2021-09-22 · Cordis - Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598C
FDA Device · Class I · 2021-09-22 · Cordis - Cordis SABER PTA Balloon Dilation Catheter, 4F, REF 48004010X
FDA Device · Class II · 2021-08-18 · Cordis - Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring percutaneous introduc…
FDA Device · Class II · 2021-07-21 · Cordis - PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC, PC0540RXC, PC0620RXC, PC0630RXC, PC0640RXC, PC0720RXC, PC…
FDA Device · Class I · 2021-03-24 · Cordis - Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S
FDA Device · Class II · 2020-03-18 · Cordis - Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use
FDA Device · Class II · 2019-11-06 · Cordis - Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduction o…
FDA Device · Class III · 2019-04-24 · Cordis - Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, in…
FDA Device · Class II · 2018-11-14 · Cordis - Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant strictures in the biliary tr…
FDA Device · Class II · 2018-01-17 · Cordis - Cordis S.M.A.R.T. Flex Vascular Stent System
FDA Device · Class II · 2017-04-26 · Cordis - Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid)
FDA Device · Class II · 2016-06-22 · Cordis - Cordis PRECISE (R) RX Nitinol Stent System (Biliary)
FDA Device · Class II · 2016-06-22 · Cordis - CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel dilator
FDA Device · Class II · 2016-03-23 · Cordis - RenLane Renal Denervation Catheter
FDA Device · Class II · 2015-08-26 · Cordis - Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal and re…
FDA Device · Class II · 2015-01-28 · Cordis - Cordis EMPIRA NC RX PTCA Dilatation Catheter
FDA Device · Class II · 2014-09-03 · Cordis - Cordis EMPIRA RX PTCA Dilatation Catheter
FDA Device · Class II · 2014-09-03 · Cordis - Cordis EMPIRA RX PTCA Dilatation Catheter Catalog # 85R30300S For cardiovascular use
FDA Device · Class II · 2014-06-18 · Cordis - Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via percutaneous placement in t…
FDA Device · Class II · 2013-11-06 · Cordis - Cordis ADROIT 6F Guiding Catheter Product Usage: For intravascular introduction of interventional and/or diagnostic devices into the corona…
FDA Device · Class II · 2013-10-09 · Cordis - Cordis OPTEASE Retrieval Inferior Vena Cava (IVC) Filter***REF Cat
FDA Device · Class I · 2013-08-14 · Cordis - FLEXSTENT Biliary Self-Expanding Stent System
FDA Device · Class II · 2013-06-12 · Cordis - FLEXSTENT Biliary Self-Expanding Stent System
FDA Device · Class II · 2013-06-12 · Cordis - FLEXSTENT Femoropopliteal Self-Expanding Stent System
FDA Device · Class II · 2013-06-12 · Cordis - FLEXSTENT Femoropopliteal Self-Expanding Stent System
FDA Device · Class II · 2013-06-12 · Cordis - FLEXSTENT Femoropopliteal Self-Expanding Stent System
FDA Device · Class II · 2013-06-12 · Cordis - Cordis, a Johnson and Johnson Company, ExoSeal(TM) 6F Vascular Closure Device, cat
FDA Device · Class II · 2013-02-06 · Cordis - Sleek OTW***REF 426-1201X***Inflated Balloon Dia/mm***1.25***Inflated Balloon Length/mm***15***Usable Catheter Length/cm***150*** Lot 50027…
FDA Device · Class II · 2012-10-03 · Cordis - Sleek ***OTW ***Ref ***426-1501X***Inflated Balloon Dia/mm 1.5 Inflated Balloon Length/mm 15 Usable Catheter Length/cm 150***Lot 50026688**…
FDA Device · Class II · 2012-10-03 · Cordis