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Medium risk Drugs & MedicationsClass II

Angiodynamics, Inc. Recall

Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN No.: H787107140145 (

Updated March 3, 2026

Angiodynamics, Inc. is recalling Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN No.: H787107140145 (. 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.

Is the Angiodynamics, Inc. recalled? Yes. This product was recalled by FDA on March 3, 2026. Details below.

What is recalled

Soft-Vu Angiographic Catheter, Kumpe, Non-Braided; SOFT-VU KMP 4F X 65CM 038 NB 0SH; Catalog No.: 10714014; Product/UPN No.: H787107140145 (Box), H787107140140 (Pouch); Box Quantity: 5 pouches;

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

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.

Brands affected

Angiodynamics, Inc.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-1862-2026
Classification
Class II
Recalled
March 3, 2026
Read the official notice

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