Vortex Surgical Inc.: Medical Device Recall in 2026 - (Recall #: Z-1004-2026)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2026.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: November 19, 2025

Date Posted: January 7, 2026

Recall Number: Z-1004-2026

Event ID: 98032

Reason for Recall:

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

Status: Ongoing

Product Quantity: 221 units

Code Information:

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

Distribution Pattern:

US and Japan

Voluntary or Mandated:

Voluntary: Firm initiated