FDA recall, , Moderate risk
D.O.R.C. TDC VELOCE Two Dimensional Cutters
TDC Veloce cutters have a loose outer knife that can become loose during use.
Summary by Recall Canary from the FDA notice
What happened
D.O.R.C. Dutch Opthalmic Research Center Intl B.V., based in Zuidland, Netherlands, recalled TDC Veloce 23G, 25G, and 27G Two Dimensional Cutters - 20k CPM due to an increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use. The recall began April 30, 2026, and was added to the FDA's Enforcement Report on June 5, 2026, with distribution nationwide and worldwide including countries such as Australia, France, Japan, and the United States.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Affected if its UDI-DI and lot code are listed under that product.
Incomplete list: 78 of 143 lot codes shown.
A UDI-DI is the device identifier printed with the barcode on the device label.
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;
- UDI-DI
- 08717872031866
- 08717872035109
- 08717872035338
- 08717872035307
- 100637001
- 85451001
- 86069001
- 86798001
- 86799001
- 87205001
- 88231001
- 91957001
- 92629001
- 92630001
- 93336001
- 94351001
- 95436001
- 95462001
- 96097001
- 96123001
- 97279001
- 97789001
- 98643001
- 99130001
- 99185001
- 99697001
- Lot code
- 57682
- 64312
- 69017
- 73237
- 74225
- 75735
- 79460
- 80338
- 80963
- 81335
- 81679
- 82213
- 82325
- 82742
- 82779
- 83584
- 84580
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;
- UDI-DI
- 08717872031880
- 08717872035123
- 08717872035352
- 08717872035321
- 202511001
- 202601070
- 85452001
- 86070001
- 87206001
- 90383001
- 97231001
- Lot code
- 51682
- 51683
- 54025
- 54995
- 56258
- 56259
- 64307
- 64310
- 69018
- 75718
- 76781
- 76810
- 77842
- 79461
- 80339
- 80964
- 81336
- 82214
- 82743
- 83585
- 84581
TDC Veloce", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;
- UDI-DI
- 08717872031873
- 08717872035116
- 08717872035345
- 101118001
- 101799001
- 101800001
- 102675001
- 102676001
- 103507001
- 103508001
- 103509001
- 104360001
- 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
- Lot code
- 101118001
- 101799001
- 101800001
- 102675001
- 102676001
- 103507001
- 103508001
- 103509001
- 104360001
- 50489
- 54992
- 54993
- 54994
- 56251
- 56254
- 56255
- 56256
- 56257
- 57683
- 58588
- 58589
- 60300
- 65315
- 65316
- 65317
- 65318
- 65319
- 65320
- 65321
- 65322
- 66818
- 70551
- 70552
- 70565
- 70566
- 70567
- 71803
- 71804
- 71805
- 71806
Recall details
- Company began the recall
- Sold in
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.
- Company
- D.O.R.C. Dutch Opthalmic Research Center Intl B.V.Zuidland, Netherlands
- Hazard
- Device defect
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98814
- Recall numbers
- Z-2322-2026 to Z-2324-2026
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
