FDAClass II · Medical device · Recall Z-2323-2026 · Recalled June 17, 2026

TDC VELOCE" recall — D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

Agency report date: June 17, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named: TDC VELOCE"
Company / brand: D.O.R.C. Dutch Opthalmic Research Center Intl B.V
Lot / serial / date codes: 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-*-*-1, 77375-*-*-1, 77501-*-*-1, 77502-*-*-1, 77503-*-*-1, 77504-*-*-1, 77505-*-*-1, 78097-*-*-1, 78098-*-*-1, 78110-*-*-1, 78111-*-*-1, 79425-*-*-1, 79426-*-*-1, 81292-*-*-1, 81293-*-*-1, 81681-*-*-1, 82172-*-*-1, 82173-*-*-1, 82174-*-*-1, 82326-*-*-1, 82702-*-*-1, 82703-*-*-1, 82704-*-*-1, 82778-*-*-1, 83543-*-*-1, 83544-*-*-1, 84535-*-*-1, 84536-*-*-1, 84537-*-*-1, 85411001, 85412001, 86024001, 86025001, 86026001, 86806001, 86807001, 87173001, 87174001, 87175001, 87390001, 87950001, 88204001, 88205001, 88552001, 88616001, 89535001, 90377001, 90378001, 90379001, 91280001, 91281001, 92631001, 92633001, 95437001, 99667001;
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.

Agency product description and boundaries

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

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

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

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: TDC VELOCE" recall status

3. Open the official notice or contact

View the official FDA enforcement record (openFDA) ↗

Official recall ID: Z-2323-2026
Brand: All D.O.R.C. Dutch Opthalmic Research Center Intl B.V recalls
Classification: Class II
Units affected: 2068 boxes totaling 12408 units
Recall status: Ongoing
Initiated: Voluntary: Firm initiated

Affected products

TDC VELOCE" recall status

Companies & origin

Recalling firm location: Zuidland, N/A, Netherlands
Firm address: Scheijdelveweg 2, N/A, N/A

Identifying details (verbatim from the notice)

Product codes / lots: 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-*-*-1, 77375-*-*-1, 77501-*-*-1, 77502-*-*-1, 77503-*-*-1, 77504-*-*-1, 77505-*-*-1, 78097-*-*-1, 78098-*-*-1, 78110-*-*-1, 78111-*-*-1, 79425-*-*-1, 79426-*-*-1, 81292-*-*-1, 81293-*-*-1, 81681-*-*-1, 82172-*-*-1, 82173-*-*-1, 82174-*-*-1, 82326-*-*-1, 82702-*-*-1, 82703-*-*-1, 82704-*-*-1, 82778-*-*-1, 83543-*-*-1, 83544-*-*-1, 84535-*-*-1, 84536-*-*-1, 84537-*-*-1, 85411001, 85412001, 86024001, 86025001, 86026001, 86806001, 86807001, 87173001, 87174001, 87175001, 87390001, 87950001, 88204001, 88205001, 88552001, 88616001, 89535001, 90377001, 90378001, 90379001, 91280001, 91281001, 92631001, 92633001, 95437001, 99667001;
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.
Firm notified the public via: Letter
FDA event ID: 98814
Recall initiated: April 30, 2026
FDA classified: June 5, 2026
FDA report date: June 17, 2026

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Verify with the official sources:

CPSC — consumer products ↗ (aggregated here)
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FDA — food, drugs, medical devices ↗ (aggregated here)
USDA FSIS — meat, poultry & processed egg products ↗ (not aggregated here)
Recalls.gov — the U.S. government’s all-agency portal ↗

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 6:00 PM UTC. Record retrieved September 15, 2026 at 6:00 PM UTC.

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