Alcon Research, Ltd. - Irvine Technology Center
FDA adverse event reports naming Alcon Research, Ltd. - Irvine Technology Center as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON RESEARCH, LTD. - IRVINE TECHNOLOGY CENTER.
- Total reports
- 10,108
- Deaths
- 2
- Injuries
- 1,501
- Malfunctions
- 8,605
Reports per year
2,48115
2,70316
2,59817
2,27318
5319
Source: FDA adverse event reports by year received, 2015–2019. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Unit, PhacofragmentationHQC8,961
- Aberrometer, OphthalmicNCF302
- Laser, OphthalmicHQF221
- Instrument, Vitreous Aspiration And Cutting, Ac-PoweredHQE220
- Cannula, Trocar, OphthalmicNGY134
- System, Imaging, Pulsed Echo, UltrasonicIYO78
- Microscope, Operating & Accessories, Ac-Powered, OphthalmicHRM73
- Powered Laser Surgical InstrumentGEX56
- Ophthalmic Femtosecond LaserOOE32
- General Surgery TrayLRO13
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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