Cordis Corporation recalls

25 recalls on record · latest: October 1, 2021

Official U.S. recall history for Cordis Corporation, compiled from official government records.

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Cordis Corporation recalls SMART FLEX 6x150 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of maligna…

October 1, 2021 · Medical device recalls Moderate risk There is a potential for distal tip dislodgement or separation.

Cordis Corporation recalls SMART FLEX 10x100 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of maligna…

October 1, 2021 · Medical device recalls Moderate risk There is a potential for distal tip dislodgement or separation.

Cordis Corporation recalls SMART FLEX 10x100 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malign…

October 1, 2021 · Medical device recalls Moderate risk There is a potential for distal tip dislodgement or separation.

Cordis Corporation recalls SMART FLEX 8x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant…

October 1, 2021 · Medical device recalls Moderate risk There is a potential for distal tip dislodgement or separation.

Cordis Corporation recalls SMART FLEX 9x60 BIL, 80cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of malignant…

October 1, 2021 · Medical device recalls Moderate risk There is a potential for distal tip dislodgement or separation.

Cordis Corporation recalls SMART FLEX 6x120 BIL, 120cm The S.M.A.R.T.¿ Flex Biliary Stent System is indicated for use in the palliation of maligna…

October 1, 2021 · Medical device recalls Moderate risk There is a potential for distal tip dislodgement or separation.

Cordis 5F UNIVERSAL FLUSH F4 SUPER TORQUE MB recalled over entrapment hazard

July 21, 2021 · Medical device recalls High risk Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Mark…

Cordis SUPER TORQUE MB 5F PIG recalled over entrapment hazard

July 21, 2021 · Medical device recalls High risk Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Mark…

Cordis SUPER TORQUE MB 5F PIG recalled over entrapment hazard

July 21, 2021 · Medical device recalls High risk Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Mark…

Cordis 5F SUPER TORQUE PIG PIGTAIL SPECIAL recalled over entrapment hazard

July 21, 2021 · Medical device recalls High risk Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Mark…

Cordis SUPER TORQUE MB 5F PIG recalled over entrapment hazard

July 21, 2021 · Medical device recalls High risk Cordis has identified that the SUPER TORQUE MB Angiographic Catheter (with Mark…

Cordis SABER PTA Balloon Dilation Catheter recalled over foreign material

July 19, 2021 · Medical device recalls Moderate risk The balloon protective sheath may potentially be contaminated with a foreign ma…

Cordis Corporation recalls Avanti¿+ Catheter Sheath Introducer - Product Usage: Is indicated for use in arterial and venous procedures requiring p…

June 9, 2021 · Medical device recalls Moderate risk The product in the packaging is larger (both inner and outer diameter) than the…

Cordis Corporation recalls PRECISE PRO RX CAROTID STENT implant system, Product Codes: PC0520RXC, PC0530RXC, PC0540RXC, PC0620RXC, PC0630RXC, PC06…

February 11, 2021 · Medical device recalls High risk Distal tip may become separated from the lumen wire in specific lots.

Cordis Corporation recalls Cordis POWERFLEX P3, PTA Dilation Catheter, REF 420-6020S

January 8, 2020 · Medical device recalls Moderate risk Cordis is recalling one (1) lot of POWERFLEX P3 PTA Dilatation Catheter due to…

Cordis Corporation recalls Cordis MAXI LD PTA Dilatation Catheter, for cardiovascular use.

October 4, 2019 · Medical device recalls Moderate risk Product was manufactured utilizing an expired inner body.

Cordis Corporation recalls Cordis Vista Brite Tip & Androit Guiding Catheters Product Usage: The guiding catheter is intended for use for intravas…

February 7, 2019 · Medical device recalls Frayed pieces of the mounting card being inside the primary packaging.

Cordis Corporation recalls Cordis POWERFLEX PRO PTA Dilatation Catheter - Product Usage: Is intended to dilate stenoses in iliac, femoral, ilio-fe…

September 5, 2018 · Medical device recalls Moderate risk Product may not meet the internal manufacturing shaft subassembly burst strengt…

Cordis Corporation recalls Cordis S.M.A.R.T. Flex Biliary Stent System Product Usage: Is indicated for use in the palliation of malignant strictur…

November 15, 2017 · Medical device recalls Moderate risk Potential for cracked luer hubs

Cordis Corporation recalls Cordis S.M.A.R.T. Flex Vascular Stent System

February 16, 2017 · Medical device recalls Moderate risk Deployment Difficulty.

Cordis Corporation recalls Cordis PRECISE (R) RX Nitinol Stent System (Biliary)

May 4, 2016 · Medical device recalls Moderate risk Inability to deploy the stent or partial stent deployment.

Cordis Corporation recalls Cordis PRECISE (R) PRO RX Nitinol Stent System (Carotid)

May 4, 2016 · Medical device recalls Moderate risk Inability to deploy the stent or partial stent deployment.

Cordis Corporation recalls CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath Introducer (CSI) and a vessel…

December 31, 2015 · Medical device recalls Moderate risk Incorrect cannula of the sheath introducer (smaller than intended).

Cordis Corporation recalls Cordis POWERFLEX PRO PTA Dilatation Catheter Intended to dilate stenoses in iliac, femoral, ilio-femoral, popliteal, in…

December 22, 2014 · Medical device recalls Moderate risk One unit from a demo lot of POWERFLEX PRO PTA Dilatation Catheter was left at a…

Cordis Corporation recalls RenLane Renal Denervation Catheter; Cat No.: D135601. Used in adults patients (>18 years) with drug resistant hypertens…

April 15, 2014 · Medical device recalls Moderate risk Potential Damage may occur to the helical tip of the RENLANE Renal Denervation…