Alcon Research, LLC - Alcon Precision Device
FDA adverse event reports naming Alcon Research, LLC - Alcon Precision Device as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON RESEARCH, LLC - ALCON PRECISION DEVICE.
- Total reports
- 6,791
- Deaths
- 0
- Injuries
- 592
- Malfunctions
- 6,199
Reports per year
4718
45319
32320
47421
46222
72423
2,40024
1,29825
61026
Source: FDA adverse event reports by year received, 2018–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Knife, OphthalmicHNN4,109
- Lens, Guide, IntraocularKYB767
- Folders And Injectors, Intraocular Lens (Iol)MSS432
- Unit, PhacofragmentationHQC372
- Cannula, OphthalmicHMX331
- Suture, Nonabsorbable, Synthetic, PolyamideGAR277
- Device, Irrigation, Ocular SurgeryKYG246
- Intraocular Pressure Lowering ImplantOGO122
- Catheter, IrrigationGBX52
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW35
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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