# FDA recall Z-2323-2026

> **D.O.R.C. Dutch Opthalmic Research Center Intl B.V.** · Class II · device recall initiated 2026-04-30.

## 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 for recall

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

## Distribution

Worldwide - US Nationwide and the countries of AUSTRALIA, AUSTRIA, BELGIUM, BULGARIA, CZECHIA, FINLAND, FRANCE, GERMANY, GREAT BRITAIN, HONG KONG, IRELAND, ITALY, JAPAN, NETHERLANDS, NEW ZEALAND, POLAND, SLOVENIA, SOUTH AFRICA, SPAIN, SWEDEN, TAIWAN, TURKEY.

## Key facts

- **Recall number:** Z-2323-2026
- **Recalling firm:** D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2026-04-30
- **Report date:** 2026-06-17

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Zuidland, N/A, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2323-2026

## Citation

> MORVS. FDA recall Z-2323-2026. Retrieved 2026-10-18 from https://api.morvs.ai/recall/Z-2323-2026. Source: US FDA. Licensed CC0.

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