Endurant IIRecalls & reported problems across all models
Medtronic, Inc. · 114 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
Endurant II models — page 2
114 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Endurant® II ETLW1628C146ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT2 reports
- Endurant® II ETBF3220C145ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1610C93ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1613C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETBF2813C124ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1628C156ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- Endurant® II ETLW1628C199ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1624C199ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1628C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETUF2814C102ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 death1 report
- Endurant® II ETLW1610C156ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1610C82ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1613C146ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
- Endurant® II ETLW1628C146ESYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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