Alcon Research, LLC - Irvine Technology Center
FDA adverse event reports naming Alcon Research, LLC - Irvine Technology Center as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON RESEARCH, LLC - IRVINE TECHNOLOGY CENTER.
- Total reports
- 12,604
- Deaths
- 0
- Injuries
- 2,291
- Malfunctions
- 10,313
Reports per year
115
417
16618
2,09519
1,05120
1,41821
1,68622
1,58123
1,82824
1,74025
1,03426
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Unit, PhacofragmentationHQC10,750
- Laser, OphthalmicHQF457
- Ophthalmic Femtosecond LaserOOE414
- Aberrometer, OphthalmicNCF339
- Instrument, Vitreous Aspiration And Cutting, Ac-PoweredHQE264
- Microscope, Operating & Accessories, Ac-Powered, OphthalmicHRM191
- Cannula, Trocar, OphthalmicNGY141
- EndoilluminatorMPA11
- System, Imaging, Pulsed Echo, UltrasonicIYO9
- General Surgery TrayLRO6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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