Class IIReported 2026-01-07

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

Recalled by Vortex Surgical Inc.

Reason for Recall

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

Recall Number

Z-1004-2026

Classification

Class II

Status

Ongoing

Category

device

Initiated

2025-11-19

Reported

2026-01-07

Distribution

US and Japan

Code Info

UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040

Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.