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Medium risk Medical DevicesClass II

Angiodynamics Soft-Vu Catheter 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' Soft-Vu Angiographic Catheter (Kumpe, non-braided) has a manufacturing defect that may block the guidewire from passing through the catheter hub. This could interfere with the device's intended use during angiographic procedures.

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; UPN/Product No. H787107140145 (Box) and H787107140140 (Pouch). Boxes contain 5 pouches.

Am I affected

You are affected if you use or have this catheter with UPN H787107140145 (box) or H787107140140 (pouch), and Catalog No. 10714014. Check the device labels and packaging for these numbers.

What to do right now

Stop using this catheter and contact Angiodynamics, Inc. directly for instructions on return or replacement. Do not use the device in any procedure until you have confirmed the status with the manufacturer.

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
Medical Devices
Recall ID
fda-Z-1862-2026
Classification
Class II
Recalled
March 3, 2026
Read the official notice

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