Class II

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

Vortex Surgical Inc. · November 19, 2025

Reason for Recall

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

Distribution

US and Japan

Quantity Affected

221 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1004-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.