Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT Recalled by Medtronic Vascular, Inc. Due to During stent graft deployment, the spindle may detach...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Medtronic Vascular, Inc. directly.
Affected Products
Endurant Stent Graft System REF/Description: ENTF2525C70EE STENT GRAFT ENTF2525C70EE ENDURANT TUBE
Quantity: 2 devices
Why Was This Recalled?
During stent graft deployment, the spindle may detach from the distal end of the spindle hypotube
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Vascular, Inc.
Medtronic Vascular, Inc. has 19 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report