Reported Jun 17, 2026 · Ongoing

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

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

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: D.O.R.C. Dutch Opthalmic Research Center Intl B.V. · Scheijdelveweg 2 · Zuidland, N/A · N/A

Is this the product you have?

  • 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
Lot codes and dates

10 of 10 products

Products covered by this recall
#BarcodesProduct as published
108717872031866Article Number: 9268.VIT23; UDI-DI: 08717872031866
208717872035109Article Number: 9311.23G01; UDI-DI: 08717872035109
308717872035338Article Number: 9311.23G02; UDI-DI: 08717872035338
4Article Number: 9311.23K01; UDI-DI: N/A
5Article Number: 9311.23K02; UDI-DI: N/A
6Article Number: 9311.23K03; UDI-DI: N/A
7Article Number: 9623.G0201; UDI-DI: N/A
8Article Number: 9623.G0202; UDI-DI: N/A
9Article Number: 9623.K0201; UDI-DI: N/A
1008717872035307Article Number: 9311.23G01-00; UDI-DI: 08717872035307; Lot Numbers: 100637001, 57682-*-*-1, 64312-*-*-1, 69017-*-*-1, 73237-*-*-1, 74225-*-*-1, 75735-*-*-1, 79460-*-*-1, 80338-*-*-1, 80963-*-*-1, 81335-*-*-1, 81679-*-*-1, 82213-*-*-1, 82325-*-*-1, 82742-*-*-1, 82779-*-*-1, 83584-*-*-1, 84580-*-*-1, 85451001, 86069001, 86798001, 86799001, 87205001, 88231001, 91957001, 92629001, 92630001, 93336001, 94351001, 95436001, 95462001, 96097001, 96123001, 97279001, 97789001, 98643001, 99130001, 99185001, 99697001
Amount recalled
314 boxes, totaling 1884 units

This recall covers 3 products

The agency filed one notice per product. You are reading one of them; the other 2 are below.

Where it was sold

  • Nationwide

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 7:34 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.