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Medium risk Drugs & MedicationsClass II

D.O.R.C. Dutch Opthalmic Research Center Intl B.V. Recall

TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03

Updated April 30, 2026

D.O.R.C. Dutch Opthalmic Research Center Intl B.V. is recalling TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03. Hazard: An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

Is the D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalled? Yes. This product was recalled by FDA on April 30, 2026. Details below.

What is recalled

TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 9311.23K02, 9311.23K03, 9623.G0201, 9623.G0202, 9623.K0201, 9311.23G01-00;

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

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

Brands affected

D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-2322-2026
Classification
Class II
Recalled
April 30, 2026
Read the official notice

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