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All Recalls

Every Endologix Recall

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

10 recalls
CriticalFDA
Endologix
ENDOLOGIX AFX/AFX2, Proximal (Aortic) Extension Endograft, Rx Only, Sterile EO, AFX Proximal Accessory, Infrarenal Model #/R...
Medical Devices·56,503 affected·Jul 31, 2018
CriticalFDA
Endologix
ENDOLOGIX AFX Endovascular AAA System, Stent Graft System, Rx Only, Sterile EO, REF: BA22-120/I20-40, BA22-100/I20-...
Medical Implants·45,304 affected·Jul 31, 2018
CriticalFDA
Endologix
ENDOLOGIX AFX2 Bifurcated Endograft System, Stent Graft System, Rx Only, Sterile EO, REF: BEA22-120/I20-40, BEA22-100/I20...
Medical Implants·13,178 affected·Jul 31, 2018
High RiskFDA
Endologix
AFX2 Endovascular AAA System Item No. Item Description F00820-01 BEA28-120/I20-40 F00820-02 BEA28-100/I20-40 F00820-03 BEA28-8...
Medical Devices·832 affected·Jan 4, 2017
High RiskFDA
Endologix
AFX Endovascular AAA System, Endoleak Type IIIA Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, E...
Medical Implants·0 affected·Dec 27, 2016
High RiskFDA
Endologix
AFX Endovascular AAA System, Endoleak Type: IIIB Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, ...
Medical Implants·4,143 affected·Dec 27, 2016
High RiskFDA
Endologix
AFX Endovascular AAA System, Endoleak Type IIIB Common Name: AFX Bifurcated and Accessory Stent Grafts Classification Name: System, E...
Medical Implants·17,139 affected·Dec 27, 2016
High RiskFDA
Endologix
AFX Endovascular AAA System, Endoleak Type IIIA Product Usage: The AFX Endovascular AAA System is intended for endovascular treatment...
Medical Devices·0 affected·Dec 27, 2016
High RiskFDA
Endologix
AFX Endovascular AAA System, Endoleak Type IIIA
Medical Devices·40,967 affected·Dec 27, 2016
High RiskFDA
Endologix
AFX Endovascular AAA System, Endoleak Type IIIB; The AFX Endovascular AAA System is intended for endovascular treatment of patients with...
Medical Devices·40,967 affected·Dec 27, 2016