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.VIT239311.23G019311.23G029311.23K019311.23K029311.23K039623.G02019623.G02029623.K02019311.23G01-00
- Lot codes and dates
10 of 10 products
Products covered by this recall # Barcodes Product as published 1 08717872031866Article Number: 9268.VIT23; UDI-DI: 08717872031866 2 08717872035109Article Number: 9311.23G01; UDI-DI: 08717872035109 3 08717872035338Article Number: 9311.23G02; UDI-DI: 08717872035338 4 Article Number: 9311.23K01; UDI-DI: N/A 5 Article Number: 9311.23K02; UDI-DI: N/A 6 Article Number: 9311.23K03; UDI-DI: N/A 7 Article Number: 9623.G0201; UDI-DI: N/A 8 Article Number: 9623.G0202; UDI-DI: N/A 9 Article Number: 9623.K0201; UDI-DI: N/A 10 08717872035307Article 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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