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Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Recalled January 7, 2026 · FDA recall Z-1004-2026 · Vortex Surgical
Hazard
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly. · FDA Class II
Units
221 units
Sold at
US and Japan
Description
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Product
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Manufacturer(s)
Vortex Surgical Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →