FDA Device recall Z-2324-2026

TDC VELOCE", 27G 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", 27G 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-2324-2026
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", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 9311.27K02, 9311.27K03, 9627.G0101, 9627.G0201, 9311.27G01-00;

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.VIT27; UDI-DI: 08717872031880; 2. Article Number: 9311.27G01; UDI-DI: 08717872035123; 3. Arti… 1. Article Number: 9268.VIT27; UDI-DI: 08717872031880; 2. Article Number: 9311.27G01; UDI-DI: 08717872035123; 3. Article Number: 9311.27G02; UDI-DI: 08717872035352; 4. Article Number: 9311.27K01; UDI-DI: N/A; 5. Article Number: 9311.27K02; UDI-DI: N/A; 6. Article Number: 9311.27K03; UDI-DI: N/A; 7. Article Number: 9627.G0101; UDI-DI: N/A; 8. Article Number: 9627.G0201; UDI-DI: N/A; 9. Article Number: 9311.27G01-00; UDI-DI: 08717872035321; Lot Numbers: 202511001, 202601070, 51682---1, 51683---1, 54025---1, 54995---1, 56258---1, 56259---1, 64307---1, 64310---1, 69018---1, 75718---1, 76781---1, 76810---1, 77842---1, 79461---1, 80339---1, 80964---1, 81336---1, 82214---1, 82743---1, 83585---1, 84581---1, 85452001, 86070001, 87206001, 90383001, 97231001;

code_info

1. Article Number: 9268.VIT27; UDI-DI: 08717872031880; 2. Article Number: 9311.27G01; UDI-DI: 08717872035123; 3. Arti…

1. Article Number: 9268.VIT27; UDI-DI: 08717872031880; 2. Article Number: 9311.27G01; UDI-DI: 08717872035123; 3. Article Number: 9311.27G02; UDI-DI: 08717872035352; 4. Article Number: 9311.27K01; UDI-DI: N/A; 5. Article Number: 9311.27K02; UDI-DI: N/A; 6. Article Number: 9311.27K03; UDI-DI: N/A; 7. Article Number: 9627.G0101; UDI-DI: N/A; 8. Article Number: 9627.G0201; UDI-DI: N/A; 9. Article Number: 9311.27G01-00; UDI-DI: 08717872035321; Lot Numbers: 202511001, 202601070, 51682-*-*-1, 51683-*-*-1, 54025-*-*-1, 54995-*-*-1, 56258-*-*-1, 56259-*-*-1, 64307-*-*-1, 64310-*-*-1, 69018-*-*-1, 75718-*-*-1, 76781-*-*-1, 76810-*-*-1, 77842-*-*-1, 79461-*-*-1, 80339-*-*-1, 80964-*-*-1, 81336-*-*-1, 82214-*-*-1, 82743-*-*-1, 83585-*-*-1, 84581-*-*-1, 85452001, 86070001, 87206001, 90383001, 97231001;

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-2324-2026%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.