Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Abre Venous Self-expanding Stent System Recalled by Medtronic Inc. Due to There is a potential for sterile package breach.
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 Inc. directly.
Affected Products
Abre Venous Self-expanding Stent System, Product Numbers: a) AB9U14080090; b) AB9U18100090; c) AB9G14100090
Quantity: 65 units
Why Was This Recalled?
There is a potential for sterile package breach.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Medtronic Inc.
Medtronic Inc. has 85 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report