TDC VELOCE" — Class II medical device recall Z-2322-2026
Ongoing recall by D.O.R.C. Dutch Opthalmic Research Center Intl B.V., reported 2026-06-17, distributed nationwide. An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose du
| Recall number | Z-2322-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | D.O.R.C. Dutch Opthalmic Research Center Intl B.V., Zuidland, N/A, Netherlands |
| Recall initiated | 2026-04-30 |
| Classified | 2026-06-05 |
| Reported by FDA | 2026-06-17 |
| Distributed | Nationwide (US) |
| Countries outside the US | AT, AU, BE, BG, CZ, DE, ES, FI, FR, GB, HK, IE, IT, JP, NL, NZ, PL, SE, SI, TR, TW, ZA |
| UPC / GTIN / UDI-DI | 08717872031866, 08717872035109, 08717872035307, 08717872035338 |
| Lot numbers | 100637001, 85451001, 86069001, 86798001, 86799001, 87205001, 88231001, 91957001, 92629001, 92630001, 93336001, 94351001, 95436001, 95462001, 96097001, 96123001, 97279001, 97789001, 98643001, 99130001, 99185001, 99697001 |
Product
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;
Reason for recall
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2322-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.