Alcon - Irvine Technology CTR
FDA adverse event reports naming Alcon - Irvine Technology CTR as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON - IRVINE TECHNOLOGY CTR.
- Total reports
- 1,558
- Deaths
- 0
- Injuries
- 317
- Malfunctions
- 1,229
Reports per year
1801
902
603
1504
1505
4806
1807
1908
6609
18910
16011
16012
29513
46214
6615
Source: FDA adverse event reports by year received, 2001–2015. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Unit, PhacofragmentationHQC1,373
- Instrument, Vitreous Aspiration And Cutting, Ac-PoweredHQE111
- Laser, OphthalmicHQF22
- Powered Laser Surgical InstrumentGEX16
- System, Imaging, Pulsed Echo, UltrasonicIYO14
- EndoilluminatorMPA14
- Device, Irrigation, Ocular SurgeryKYG3
- Blade, ScalpelGES1
- Motor, Surgical Instrument, Ac-PoweredGEY1
- Photocoagulator And AccessoriesHQB1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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