Health & Personal Care
HIGH
FDA DEVICE
GORE ACUSEAL Vascular Graft Recall Affects 52,306 Devices Worldwide (2025)
Gore recalled 52,306 Gore ACUSEAL Vascular Grafts distributed through healthcare providers in the United States and internationally after reports of graft delamination. Delamination may reduce access flow, cause cannulation difficulties, bleeding or bruising, and may require reinterventions. Healthcare facilities and patients should stop using the device immediately and follow the recall guidance.
Gore
Reports of