Alcon - Irvine Technology Center
FDA adverse event reports naming Alcon - Irvine Technology Center as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON - IRVINE TECHNOLOGY CENTER.
- Total reports
- 10,801
- Deaths
- 3
- Injuries
- 3,079
- Malfunctions
- 7,665
Reports per year
28101
27402
17703
17604
14105
27906
35907
33308
37909
1,93710
1,33411
1,63112
1,65813
1,49214
20315
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, PhacofragmentationHQC8,727
- Instrument, Vitreous Aspiration And Cutting, Ac-PoweredHQE1,468
- Laser, OphthalmicHQF153
- Powered Laser Surgical InstrumentGEX145
- System, Imaging, Pulsed Echo, UltrasonicIYO123
- EndoilluminatorMPA111
- Device, Irrigation, Ocular SurgeryKYG27
- Laser, Neodymium:Yag, Ophthalmic For Posterior Capsulotomy And Cutting PupillaLXS10
- Device, Medical Examination, Ac PoweredKZF7
- Stimulator, Spinal-Cord, Totally Implanted For Pain ReliefLGW4
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Alcon - Irvine Technology Center automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.