Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;

Recall date

November 19, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1004-2026

FDA classification

Class II

Brand / firm

Vortex Surgical Inc.

Sold / distributed

US and Japan

Why it was recalled

Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;