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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 complaints.

What to do

Stop using the affected device immediately. Contact D.O.R.C. for instructions on returning the product and obtaining a replacement.

Posted
Updated
Recall No.
Z-2322-2026
Agency
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. Dutch Opthalmic Research Center is recalling the TDC VELOCE 23G Two Dimensional Cutter due to an increase in complaints of a loose outer knife and reports of the outer knife becoming loose during use.

Is mine affected?

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

ProductUPCRecall #
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;08717872031866, 08717872035109, 08717872035338, 08717872035307, 100637001, 85451001, 86069001, 86798001, 86799001, 87205001, 88231001, 91957001, 92629001, 92630001, 93336001, 94351001, 95436001, 95462001, 96097001, 96123001Z-2322-2026
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;08717872031880, 08717872035123, 08717872035352, 08717872035321, 202511001, 202601070, 85452001, 86070001, 87206001, 90383001, 97231001Z-2324-2026
TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 9311.25K02, 9311.25K03, 9625.G0201;08717872031873, 08717872035116, 08717872035345, 101118001, 101799001, 101800001, 102675001, 102676001, 103507001, 103508001, 103509001, 104360001, 85411001, 85412001, 86024001, 86025001, 86026001, 86806001, 86807001, 87173001Z-2323-2026

Where it was sold

Distributed nationwide.

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Editorial summary by Recall Canary · last updated 2026-07-28 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification