Fresh Recalls

W L Gore & Associates recalls

3 recent recalls on record for W L Gore & Associates in connected official government data as of September 7, 2026 at 6:00 AM UTC.

Models with recalls

GORE VIABIL Short Wire Biliary Endoprosthesis (2)GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region (1)

All W L Gore & Associates recalls

FDA Class II · Medical device · August 19, 2026

GORE VIABIL Short Wire Biliary Endoprosthesis recall — W L Gore & Associates, Inc.

10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).

Official ID Z-2915-2026 · Official record ↗

FDA Class II · Medical device · August 19, 2026

GORE VIABIL Short Wire Biliary Endoprosthesis recall — W L Gore & Associates, Inc.

10 mm diameter x 7 cm with transmural drainage holes (VSWVH1006) incorrectly labeled as 10 mm diameter x 10 cm length devices without transmural drainage holes (VSWVN1010).

Official ID Z-2914-2026 · Official record ↗

FDA Class II · Medical device · July 8, 2026

GORE¿ TAG¿ Thoracic Branch Endoprosthesis Side Branch Component Catalog Numbers (by Region recall — W L Gore & Associates, Inc.

Due to catheter separation

Official ID Z-2672-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked September 7, 2026 at 6:00 AM UTC.