AccuVu Angiographic Catheter: recall status

⚠ Recalls found. AccuVu Angiographic Catheter is named in 4 official recalls in our current data:

• FDA Class II recall Z-1872-2026 — The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
• FDA Class II recall Z-1873-2026 — The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
• FDA Class II recall Z-1874-2026 — The affected devices contain a manufacturing defect which may prevent the appropriately sized guidewire from passing through the inner diameter (ID) of the catheter hub.
• And 1 more listed below.