FDAMarch 3, 2026device

Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.: 10734301; Product/UPN No.: H787107343015 (Box), H787107343010 (Pouch); Box Quantity: 5 pouches;

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

angiodynamics

UPCs

2505168401011215051684010115

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 035 NB 0SH; Catalog No.: 10734301; Product/UPN No.: H787107343015 (Box), H787107343010 (Pouch); Box Quantity: 5 pouches; — Recall Details · AllClear