FDA Device recall Z-2323-2026

TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM

FDA Device
Class II
ongoing
Published 2026-06-17

On 2026-06-17 the FDA classified a Class II recall of TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM by D O R C Dutch Opthalmic Research Center Intl B V, citing an increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2323-2026
Classification	Class II
Status	ongoing
Initiated	2026-04-30
Published	2026-06-17
Last updated	2026-09-13 11:58 UTC
Company	D O R C Dutch Opthalmic Research Center Intl B V
Distribution	US

Product

TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;

Reason

An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

Identifiers

code_info	1. Article Number: 9268.VIT25; UDI-DI: 08717872031873; 2. Article Number: 9311.25G01; UDI-DI: 08717872035116; 3. Arti… 1. Article Number: 9268.VIT25; UDI-DI: 08717872031873; 2. Article Number: 9311.25G01; UDI-DI: 08717872035116; 3. Article Number: 9311.25G02; UDI-DI: 08717872035345; 4. Article Number: 9311.25K01; UDI-DI: N/A; 5. Article Number: 9311.25K02; UDI-DI: N/A; 6. Article Number: 9311.25K03; UDI-DI: N/A; 7. Article Number: 9625.G0201; UDI-DI: N/A; Lot Numbers: 101118001, 101799001, 101800001, 102675001, 102676001, 103507001, 103508001, 103509001, 104360001, 50489---1, 54992---1, 54993---1, 54994---1, 56251---1, 56254---1, 56255---1, 56256---1, 56257---1, 57683---1, 58588---1, 58589---1, 60300---1, 65315---1, 65316---1, 65317---1, 65318---1, 65319---1, 65320---1, 65321---1, 65322---1, 66818---1, 70551---1, 70552---1, 70565---1, 70566---1, 70567---1, 71803---1, 71804---1, 71805---1, 71806---1, 75717---1, 76191---1, 76516---1, 76806---1, 76807---1, 76808---1, 76852---1, 76853---1, 76854---1, 76855---1, 77374---

code_info

1. Article Number: 9268.VIT25; UDI-DI: 08717872031873; 2. Article Number: 9311.25G01; UDI-DI: 08717872035116; 3. Arti…

1. Article Number: 9268.VIT25; UDI-DI: 08717872031873; 2. Article Number: 9311.25G01; UDI-DI: 08717872035116; 3. Article Number: 9311.25G02; UDI-DI: 08717872035345; 4. Article Number: 9311.25K01; UDI-DI: N/A; 5. Article Number: 9311.25K02; UDI-DI: N/A; 6. Article Number: 9311.25K03; UDI-DI: N/A; 7. Article Number: 9625.G0201; UDI-DI: N/A; Lot Numbers: 101118001, 101799001, 101800001, 102675001, 102676001, 103507001, 103508001, 103509001, 104360001, 50489-*-*-1, 54992-*-*-1, 54993-*-*-1, 54994-*-*-1, 56251-*-*-1, 56254-*-*-1, 56255-*-*-1, 56256-*-*-1, 56257-*-*-1, 57683-*-*-1, 58588-*-*-1, 58589-*-*-1, 60300-*-*-1, 65315-*-*-1, 65316-*-*-1, 65317-*-*-1, 65318-*-*-1, 65319-*-*-1, 65320-*-*-1, 65321-*-*-1, 65322-*-*-1, 66818-*-*-1, 70551-*-*-1, 70552-*-*-1, 70565-*-*-1, 70566-*-*-1, 70567-*-*-1, 71803-*-*-1, 71804-*-*-1, 71805-*-*-1, 71806-*-*-1, 75717-*-*-1, 76191-*-*-1, 76516-*-*-1, 76806-*-*-1, 76807-*-*-1, 76808-*-*-1, 76852-*-*-1, 76853-*-*-1, 76854-*-*-1, 76855-*-*-1, 77374-*-*-

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2323-2026%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.