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TDC VELOCE 23G Two Dimensional Cutter
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MEDICAL DEVICE RECALLMODERATE

TDC VELOCE 23G Two Dimensional Cutter

D.O.R.C. recalls TDC VELOCE 23G cutter over loose outer knife risk.

What to do

Do not use the affected TDC VELOCE 23G Two Dimensional Cutter. Contact D.O.R.C. for instructions on returning the device and obtaining a replacement.

Recalled
Listed
Updated
Recall No.
Z-2322-2026
Agency
FDA
Firm
D.O.R.C. Dutch Opthalmic Research Center Intl B.V.
Recall ID
98814
Status
ONGOING

Why it was recalled

D.O.R.C. is recalling the TDC VELOCE 23G Two Dimensional Cutter due to an increased incidence of complaints of a loose outer knife and reports of the outer knife becoming loose during use, which may cause tissue damage or injury. The affected article numbers are listed in the product identifier.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

ProductLot codeRecall #UDI-DI
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;100637001, 57682, 64312, 69017, 73237, 74225, 75735, 79460, 80338, 80963, 81335, 81679, 82213, 82325, 82742, 82779, 83584, 84580, 85451001, 86069001, 86798001, 86799001, 87205001, 88231001, 91957001, 92629001, 92630001, 93336001, 94351001, 95436001, 95462001, 96097001, 96123001, 97279001, 97789001, 98643001, 99130001, 99185001, 99697001Z-2322-202608717872031866, 08717872035109, 08717872035338, 08717872035307, 100637001, 85451001, 86069001, 86798001, 86799001, 87205001, 88231001, 91957001, 92629001, 92630001, 93336001, 94351001, 95436001, 95462001, 96097001, 96123001
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;202511001, 202601070, 51682, 51683, 54025, 54995, 56258, 56259, 64307, 64310, 69018, 75718, 76781, 76810, 77842, 79461, 80339, 80964, 81336, 82214, 82743, 83585, 84581, 85452001, 86070001, 87206001, 90383001, 97231001Z-2324-202608717872031880, 08717872035123, 08717872035352, 08717872035321, 202511001, 202601070, 85452001, 86070001, 87206001, 90383001, 97231001
TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;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 (+65 more, see the official notice)Z-2323-202608717872031873, 08717872035116, 08717872035345, 101118001, 101799001, 101800001, 102675001, 102676001, 103507001, 103508001, 103509001, 104360001, 85411001, 85412001, 86024001, 86025001, 86026001, 86806001, 86807001, 87173001

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-09-08 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification