Alcon Research, Ltd. - Alcon Precision Device
FDA adverse event reports naming Alcon Research, Ltd. - Alcon Precision Device as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON RESEARCH, LTD. - ALCON PRECISION DEVICE.
- Total reports
- 1,852
- Deaths
- 0
- Injuries
- 119
- Malfunctions
- 1,733
Reports per year
38815
45316
50817
48318
2019
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
- Knife, OphthalmicHNN1,611
- Lens, Guide, IntraocularKYB112
- Device, Irrigation, Ocular SurgeryKYG35
- Cannula, OphthalmicHMX34
- Unit, PhacofragmentationHQC29
- Suture, Nonabsorbable, Synthetic, PolyamideGAR13
- Catheter, IrrigationGBX10
- Intraocular Pressure Lowering ImplantOGO5
- Suture, Nonabsorbable, SilkGAP1
- General Surgery TrayLRO1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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