Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GORE TAG Conformable Thoracic Stent Graft with ACTIVE CONTROL System Recalled by W L Gore & Associates, Inc. Due to When the delivery catheter was attempted to be...
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 W L Gore & Associates, Inc. directly.
Affected Products
GORE TAG Conformable Thoracic Stent Graft with ACTIVE CONTROL System
Quantity: 19013 units
Why Was This Recalled?
When the delivery catheter was attempted to be removed, there was an observed connection between the stent graft and the delivery catheter that prevented the delivery catheter from being withdrawn.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About W L Gore & Associates, Inc.
W L Gore & Associates, Inc. has 21 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report