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Cordis Corporation Recalls

26 recalls on record. Search official CPSC, FDA, and USDA datasets for every recall issued for Cordis Corporation.

26Total Recalls
4Critical
412,694Units Affected
Oct 1, 2021Most Recent
All Recalls

Every Cordis Corporation Recall

Sorted by most recent. Click any recall for full details.

26 recalls
High RiskFDA
Cordis Corporation
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 ...
Medical Implants·26 affected·Oct 1, 2021
High RiskFDA
Cordis Corporation
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 ...
Medical Implants·4 affected·Oct 1, 2021
High RiskFDA
Cordis Corporation
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...
Medical Implants·4 affected·Oct 1, 2021
High RiskFDA
Cordis Corporation
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 th...
Medical Implants·4 affected·Oct 1, 2021
High RiskFDA
Cordis Corporation
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 th...
Medical Implants·9 affected·Oct 1, 2021
CriticalFDA
Cordis Corporation
Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB, SPECIAL, Angiographic Catheter, REF SRD6785MB
Surgical Devices·45 affected·Jul 21, 2021
CriticalFDA
Cordis Corporation
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598C
Surgical Devices·26,025 affected·Jul 21, 2021
CriticalFDA
Cordis Corporation
Cordis SUPER TORQUE MB 5F PIG, Angiographic Catheter, REF 532-598B
Surgical Devices·71,330 affected·Jul 21, 2021
CriticalFDA
Cordis Corporation
Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL, Angiographic Catheter, REF SRD7040MB
Surgical Devices·1,610 affected·Jul 21, 2021
High RiskFDA
Cordis Corporation
Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring percutaneous introd...
Surgical Devices·680 affected·Jun 9, 2021
RecallFDA
Cordis Corporation
Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravascular introduc...
Surgical Devices·23,481 affected·Feb 7, 2019
High RiskFDA
Cordis Corporation
Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, ...
Medical Implants·162 affected·Sep 5, 2018
High RiskFDA
Cordis Corporation
Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant strictures in the bili...
Medical Implants·511 affected·Nov 15, 2017
High RiskFDA
Cordis Corporation
Cordis PRECISE (R) RX Nitinol Stent System (Biliary)
Medical Implants·4,400 affected·May 4, 2016
High RiskFDA
Cordis Corporation
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel dilator. A Cath...
Surgical Devices·1,985 affected·Dec 31, 2015
High RiskFDA
Cordis Corporation
Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, infra popliteal a...
Medical Implants·120 affected·Dec 22, 2014
High RiskFDA
Cordis Corporation
Cordis EMPIRA NC RX PTCA Dilatation Catheter
Surgical Devices·250,000 affected·Jun 23, 2014
High RiskFDA
Cordis Corporation
RenLane Renal Denervation Catheter; Cat No.: D135601. Used in adults patients (>18 years) with drug resistant hypertension to denervate ...
Surgical Devices·98 affected·Apr 15, 2014
High RiskFDA
Cordis Corporation
Cordis OPTEASE Vena Cava Filter Is indicated for use in the prevention of recurrent pulmonary embolism (PE) via percutaneous placement...
Medical Devices·29,395 affected·Sep 27, 2013
High RiskFDA
Cordis Corporation
FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for use in the pall...
Medical Implants·23 affected·Apr 23, 2013
High RiskFDA
Cordis Corporation
FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT¿ Femoropopliteal SES clinical product is ind...
Medical Implants·784 affected·Apr 23, 2013
High RiskFDA
Cordis Corporation
FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT¿ Femoropopliteal SES clinical product is ind...
Medical Implants·310 affected·Apr 23, 2013
High RiskFDA
Cordis Corporation
FLEXSTENT Femoropopliteal Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT¿ Femoropopliteal SES clinical product is ind...
Medical Implants·250 affected·Apr 23, 2013
High RiskFDA
Cordis Corporation
FLEXSTENT Biliary Self-Expanding Stent System. Product Usage: The FSS FLEXSTENT Biliary SES product is indicated for use in the pall...
Medical Implants·1,357 affected·Apr 23, 2013
High RiskFDA
Cordis Corporation
Cordis EMPIRA RX PTCA Dilatation Catheter Catalog # 85R30300S For cardiovascular use.
Surgical Devices·80 affected·Feb 5, 2013
High RiskFDA
Cordis Corporation
Sleek ***OTW ***Ref ***426-1501X***Inflated Balloon Dia/mm 1.5 Inflated Balloon Length/mm 15 Usable Catheter Length/cm 150***Lot 50026688...
Surgical Devices·1 affected·Jan 31, 2011