Reported Jun 17, 2026 · Ongoing

TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01,…

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", 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
Lot codes and dates

9 of 9 products

Products covered by this recall
#BarcodesProduct as published
108717872031880Article Number: 9268.VIT27; UDI-DI: 08717872031880
208717872035123Article Number: 9311.27G01; UDI-DI: 08717872035123
308717872035352Article Number: 9311.27G02; UDI-DI: 08717872035352
4Article Number: 9311.27K01; UDI-DI: N/A
5Article Number: 9311.27K02; UDI-DI: N/A
6Article Number: 9311.27K03; UDI-DI: N/A
7Article Number: 9627.G0101; UDI-DI: N/A
8Article Number: 9627.G0201; UDI-DI: N/A
908717872035321Article 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
Amount recalled
261 boxes totaling 1566 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, 5:42 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.