Medical Device Recall: 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;
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. · April 30, 2026
Reason for Recall
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
Distribution
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.
States Affected
NATIONWIDE
Quantity Affected
314 boxes, totaling 1884 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2322-2026
Status: ongoing
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