FDAMarch 3, 2026device

Soft -Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 40CM 038 NB 0SH; Catalog No.: 10710013; Product/UPN No.: H787107100135 (Box), H787107100130 (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

2505168400744015051684007443

Recall history

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

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