ClearanceBrief
Recall Z-2322-2026 ยท HQE Instrument, Vitreous Aspiration And Cutting, Ac-Powered

D.O.R.C. Dutch Opthalmic Research Center Intl B.V.

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;

DateJun 5, 2026 (initiated Apr 30, 2026)
StatusOpen, Classified
ReasonAn increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Root causeProcess design
ActionOn April 30, 2026 Urgent Medical Device Recall letters were sent to customers. Actions to be taken: Review this Product information as soon as possible with relevant members of your staff. 1. Pass this FSN as soon as possible on to all those who need to be aware of it, including other locations, organizations and/or customers who might have received the impacted Product(s) through you. 2. If you have the affected Products and the affected lots (see attachment below) in your inventory, remove and return them to DORC following the instructions in the attachment. 3. Follow the instructions on ho
Quantity314 boxes, totaling 1884 units
DistributionWorldwide - 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.
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K213467EVA NEXUS Ophthalmic Surgical System
D.O.R.C. Dutch Ophthalmic Research Center (International), Jun 14, 2022