HIGHFDA DEVICE
W L Gore & Associates Recalls Vascular Grafts Over Delamination Risk
W L Gore & Associates recalled over 52,000 vascular grafts on August 26, 2025, due to reports of delamination. The defect can lead to severe complications such as bleeding or cannulation difficulties. Affected products include multiple model numbers, which were distributed across the United States and internationally.
W L Gore & Associates
Reports of