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
- 12,431
- Deaths
- 0
- Injuries
- 2,223
- Malfunctions
- 10,208
Reports per year
115
417
16618
2,09519
1,05120
1,41821
1,68622
1,58123
1,82824
1,74025
86126
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Unit, PhacofragmentationHQC10,614
- Laser, OphthalmicHQF455
- Ophthalmic Femtosecond LaserOOE410
- Aberrometer, OphthalmicNCF330
- Instrument, Vitreous Aspiration And Cutting, Ac-PoweredHQE260
- Microscope, Operating & Accessories, Ac-Powered, OphthalmicHRM187
- Cannula, Trocar, OphthalmicNGY128
- 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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