FDAFebruary 27, 2017device

Endurant / Endurant II 23mm and 25mm Bifurcated Stent Graft Systems Model Numbers: ETBF2516C145E ETBF2516C166E ETBF2316C145E ETBF2313C145E ETBF2513C166E ETBF2313C166E ETBF2316C166E ETBF2313C124E ETBF2513C145E ETBF2516C124E ETBF2316C124E ETBF2513C124E. Cardiology: The Endurant family of stent graf...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Medtronic is initiating a voluntary Urgent Medical Device Recall for a subset of Endurant/ Endurant II Bifurcated Stent Graft Systems of specific models and serial numbers as this specific subset of stent grafts has greater susceptibility to fabric permeability variations that may be associated with endoleaks observed during the initial implant procedure.

What to do

FDA enforcement status: Terminated

Brands named

medtronic vascularmedtronic

UPCs

006139949920480064316921584900613994992024006431692158560061399499126300643169215795006139949919800061399499203100613994644268006431692158320061399464425100643169215788

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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