Skip to content
Recall Observatory FDA recall evidence

Device product

Endurant II/Endurant IIs Stent Graft System: Medtronic Endurant II Stent Graft System REF ETUF3214C102EE, ETCF3636C49EE, ETBF3216C166EE, and ETUF3614C102E. Used to treat infrarenal abdominal aortic or aortoiliac aneurysms using an endovascular approach.

Z-2135-2021

June 07, 2021

Class II

Product summary

Firm
Medtronic Vascular, Inc.
Event
Event 88158
Status
Ongoing
Classification
Class II
Quantity
18 devices
Official record key
device-enforcement:Z-2135-2021

Official wording

Reason: During stent graft deployment, the radiopaque (RO) marker bond detached from the distal end of the graft cover.

Code information: Endurant II Stent Graft System: Model (REF): ETCF3636C49EE GTIN: 00763000099626 Serial Numbers: V29778214; V29778215; Model (REF): ETUF3214C102EE GTIN: 00643169780958 Serial Numbers: V29775791; V29775792; V29775793; V29775794; V29775795; Model (REF): ETBF3216C166EE GTIN: 00763000099626 Serial Numbers: V29778214; V29778215; Model (REF): ETUF3614C102E GTIN: 00643169232631 Serial Numbers: V29781886 V29781883 V29781889 V29781887 V29781890 V29781891 V29781882

Distribution pattern: U.S.: GA, MA, MD, NY, SC, TX, WA, and WV O.U.S.: Argentina, Australia, Germany, Greece, Israel, Italy, Netherlands, Poland, South Africa, Spain, Switzerland and United Kingdom.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    During stent graft deployment, the radiopaque (RO) marker bond detached from the distal end of the graft cover.