Soft-Vu Angiographic Catheter: recall status

⚠ Recalls found. Soft-Vu Angiographic Catheter is named in 16 official recalls in our current data:

• FDA Class II recall Z-1856-2026 — 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-1857-2026 — 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-1858-2026 — 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 13 more listed below.