Official recall notice
FDA DeviceClass IINotable
FDA Recall: Soft-Vu Angiographic Catheter, Pigtail, Non-Braided; SOFT-VU PT 4F X 65CM 038 NB 10SH; Catalog No.
- Recall date
- 2026-04-29
- Brand
- Angiodynamics, Inc.
- Category
- Medical Device
- FDA class
- Class II
Why it was recalled
Hazard
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.
Recommended action
What to do
950 units (95 boxes)
Product description
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.