Home / Brands / D.O.R.C. Dutch Opthalmic Research Center Intl B.V
D.O.R.C. Dutch Opthalmic Research Center Intl B.V Recalls
6 recalls on record · March 27, 2024 to June 17, 2026 · Medical Devices
Recalls by year
24
26
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
June 17, 2026Medical DevicesFDA
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls TDC VELOCE", 27G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT27, 9311.27G01, 9311.27G02, 9311.27K01, 931
Hazard: An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
June 17, 2026Medical DevicesFDA
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls TDC VELOCE", 25G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, 931
Hazard: An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
June 17, 2026Medical DevicesFDA
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls TDC VELOCE", 23G Two Dimensional Cutter - 20k CPM; Article Numbers: 9268.VIT23, 9311.23G01, 9311.23G02, 9311.23K01, 931
Hazard: An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
March 27, 2024Medical DevicesFDA
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls Directional Laser Probe with Alcon / Lumenis connector (27 gauge / 0.4 mm)
Hazard: When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.
March 27, 2024Medical DevicesFDA
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls Directional Laser Probe with Alcon / Lumenis connector (25 gauge / 0.5 mm)
Hazard: When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.
March 27, 2024Medical DevicesFDA
D.O.R.C. Dutch Opthalmic Research Center Intl B.V. recalls Directional Laser Probe with Alcon / Lumenis connector (23 gauge / 0.6 mm)
Hazard: When using those products you may experience difficulties to extend or retract the laser fiber, and in some occasions may also have difficulties to direct the laser fiber tip precisely.