Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1864-2026 — Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog No.: 10714017; Product/UPN No.: H787107140175 (Box), H787107140170 (Pouch); Box Quantity: 5 pouches;

U.S. FDA — Device Enforcement · United States · 2026-03-03 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1864-2026
Date of alert: 2026-03-03
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Angiodynamics, Inc.
Product category: device
Product type: Devices
Barcode (EAN/GTIN): 10714017

Reported risk: 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.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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Recall Z-1864-2026 — Soft-Vu Angiographic Catheter, Cobra (1), Non-Braided; SOFT-VU CB1 4F X 100CM 038 NB 0SH; Catalog No.: 10714017; Product/UPN No.: H787107140175 (Box), H787107140170 (Pouch); Box Quantity: 5 pouches;

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