Alcon Lensx, Inc.
FDA adverse event reports naming Alcon Lensx, Inc. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: ALCON LENSX, INC..
- Total reports
- 1,747
- Deaths
- 0
- Injuries
- 978
- Malfunctions
- 769
Reports per year
213
114
18415
36016
33117
27918
10819
6820
5321
5022
5023
9924
12825
3426
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
- 2014-04-09TerminatedDevice Design
Alcon LenSx Ophthalmic Laser, for use in cataract surgery for the creation of corneal cuts/incisions, anterior capsulotomy and laser phacofragmentation.
Alcon LenSx received reports of unexpected downward motion of the gantry.
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