ACRYSOFRecalls & reported problems across all models
Alcon Laboratories, Inc. · 353 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
ACRYSOF models — page 2
353 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- ACRYSOF® SN6AT4intraocular lens4 reports
- ACRYSOF® SN6AT4intraocular lens4 reports
- ACRYSOF® SN6AT5intraocular lens4 reports
- ACRYSOF® SN6AT5intraocular lens4 reports
- ACRYSOF® SN6AT5intraocular lens4 reports
- ACRYSOF® SN6AT5intraocular lens4 reports
- ACRYSOF® SN6AT6intraocular lens4 reports
- ACRYSOF® SA60WFintraocular lens4 reports
- ACRYSOF® SA60ATintraocular lens4 reports
- ACRYSOF® SN60WFintraocular lens4 reports
- ACRYSOF® SN60WFintraocular lens4 reports
- ACRYSOF® SN60WFintraocular lens4 reports
- ACRYSOF® SA60ATintraocular lens3 reports
- ACRYSOF® SN60ATintraocular lens3 reports
- ACRYSOF® SN60ATintraocular lens3 reports
- ACRYSOF® SN60ATintraocular lens3 reports
- ACRYSOF® SN60ATintraocular lens3 reports
- ACRYSOF® SN60ATintraocular lens3 reports
- ACRYSOF® SN60ATintraocular lens3 reports
- ACRYSOF® SN6AT3intraocular lens3 reports
- ACRYSOF® SN6AT3intraocular lens3 reports
- ACRYSOF® SN6AT3intraocular lens3 reports
- ACRYSOF® SN6AT3intraocular lens3 reports
- ACRYSOF® SN6AT4intraocular lens3 reports
- ACRYSOF® SN6AT4intraocular lens3 reports
- ACRYSOF® SN6AT4intraocular lens3 reports
- ACRYSOF® SN6AT4intraocular lens3 reports
- ACRYSOF® SN6AT4intraocular lens3 reports
- ACRYSOF® SN6AT5intraocular lens3 reports
- ACRYSOF® SN6AT5intraocular lens3 reports
- ACRYSOF® SN6AT5intraocular lens3 reports
- ACRYSOF® SN6AT6intraocular lens3 reports
- ACRYSOF® SN6AT9intraocular lens3 reports
- ACRYSOF® SA60WFintraocular lens3 reports
- ACRYSOF® SA60WFintraocular lens3 reports
- ACRYSOF® SA60WFintraocular lens3 reports
- ACRYSOF® SA60ATintraocular lens3 reports
- ACRYSOF® SA60ATintraocular lens3 reports
- ACRYSOF® SA60ATintraocular lens3 reports
- ACRYSOF® SA60ATintraocular lens3 reports
- ACRYSOF® SA60ATintraocular lens3 reports
- ACRYSOF® SN60WFintraocular lens3 reports
- ACRYSOF® SN60WFintraocular lens3 reports
- ACRYSOF® SN60WFintraocular lens3 reports
- ACRYSOF® SN60WFintraocular lens3 reports
- ACRYSOF® SN60WFintraocular lens3 reports
- ACRYSOF® SN60WFintraocular lens3 reports
- ACRYSOF® SA60ATintraocular lens2 reports
- ACRYSOF® SN60ATintraocular lens2 reports
- ACRYSOF® SN60ATintraocular lens2 reports
- ACRYSOF® SN60ATintraocular lens2 reports
- ACRYSOF® SN60ATintraocular lens2 reports
- ACRYSOF® SN60ATintraocular lens2 reports
- ACRYSOF® SN60ATintraocular lens2 reports
- ACRYSOF® SN60ATintraocular lens2 reports
- ACRYSOF® SN6AT3intraocular lens2 reports
- ACRYSOF® SN6AT3intraocular lens2 reports
- ACRYSOF® SN6AT4intraocular lens2 reports
- ACRYSOF® SN6AT4intraocular lens2 reports
- ACRYSOF® SN6AT4intraocular lens2 reports
- ACRYSOF® SN6AT4intraocular lens2 reports
- ACRYSOF® SN6AT4intraocular lens2 reports
- ACRYSOF® SN6AT4intraocular lens2 reports
- ACRYSOF® SN6AT5intraocular lens2 reports
- ACRYSOF® SN6AT5intraocular lens2 reports
- ACRYSOF® SN6AT5intraocular lens2 reports
- ACRYSOF® SN6AT6intraocular lens2 reports
- ACRYSOF® SN6AT6intraocular lens2 reports
- ACRYSOF® SN6AT6intraocular lens2 reports
- ACRYSOF® SN6AT6intraocular lens2 reports
- ACRYSOF® SN6AT6intraocular lens2 reports
- ACRYSOF® SN6AT6intraocular lens2 reports
- ACRYSOF® SN6AT6intraocular lens2 reports
- ACRYSOF® SN6AT7intraocular lens2 reports
- ACRYSOF® SN6AT7intraocular lens2 reports
- ACRYSOF® SN6AT7intraocular lens2 reports
- ACRYSOF® SN6AT8intraocular lens2 reports
- ACRYSOF® SN6AT8intraocular lens2 reports
- ACRYSOF® SN6AT9intraocular lens2 reports
- ACRYSOF® SN6AT9intraocular lens2 reports
- ACRYSOF® SN6AT9intraocular lens2 reports
- ACRYSOF® SA60WFintraocular lens2 reports
- ACRYSOF® SA60WFintraocular lens2 reports
- ACRYSOF® SA60WFintraocular lens2 reports
- ACRYSOF® SA60WFintraocular lens2 reports
- ACRYSOF® SA60WFintraocular lens2 reports
- ACRYSOF® SA60WFintraocular lens2 reports
- AcrySof® SA6AT6intraocular lens2 reports
- ACRYSOF® SA60ATintraocular lens2 reports
- ACRYSOF® SA60ATintraocular lens2 reports
- ACRYSOF® SA60ATintraocular lens2 reports
- ACRYSOF® SA60ATintraocular lens2 reports
- ACRYSOF® SA60ATintraocular lens2 reports
- ACRYSOF® SA60ATintraocular lens2 reports
- ACRYSOF® SA60ATintraocular lens2 reports
- ACRYSOF® SN60WFintraocular lens2 reports
- ACRYSOF® SN60WFintraocular lens2 reports
- ACRYSOF® SN60WFintraocular lens2 reports
- ACRYSOF® SA60ATintraocular lens1 report
- ACRYSOF® SA60ATintraocular lens1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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