Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
GORE TAG Recalled by W L Gore & Associates, Inc. Due to Incomplete and/or partial deployment of the CTAG Device...
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, THORACIC ENDOPROSTHESIS, CONFORMABLE. The GORE TAG Thoracic Endoprosthesis is intended for endovascular repair of all lesions of the descending thoracic aorta.
Quantity: 12,197units
Why Was This Recalled?
Incomplete and/or partial deployment of the CTAG Device during the endovascular procedure.
Where Was This Sold?
Worldwide.
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