ACRYSOF® SN6AT6 (REF SN6AT6U230)Recalls & reported problems
Alcon Laboratories, Inc. · AcrySof(R) IQ TORIC ASTIGMATISM IOL, SINGLE-PIECE ACRYLIC FOLDABLE LENS, UV WITH BLUE LIGHTFILTER, 13.0mm LENGTH, 6.0mm BICONVEX TORICASPHERIC OPTIC, 3.75 D CYLINDER. · Class 3 · Implant
All models of ACRYSOF (353)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00380652274920), received between May 25, 2021 and May 25, 2021 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Excessive Tear Production1
- Eye Pain1
- Iritis1
- Red Eye(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 25, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A CONSUMERS WIFE REPORTED THAT FOLLOWING A CATARACT SURGERY WITH AN INTRAOCULAR LENS (IOL) IMPLANTATION, HER HUSBAND IS EXPERIENCING PROBLEMS/ADVERSE EVENTS WITH AN IOL. ADDITIONAL INFORMATION WAS PROVIDED INDICATING THAT HER HUSBAND'S RIGHT EYE SEEMS TO BE RED AND WATERY. HE HAS SEEN THE DOCTOR AND THEY DIDN'T SEE ANYTHING WRONG WITH THE LENS BUT THOUGHT HE MAY HAVE SLIGHT IRRITATION AND PROVIDED HIM ANTIBIOTIC DROPS. SHE REPORTED THAT HIS SYMPTOMS ARE RECENT AND AFTER SURGERY HE WAS FINE AND DID NOT HAVE ANY CONCERNS. HE IS NOT HAVING ANY VISUAL CONCERNS. ADDITIONAL INFORMATION WAS PROVIDED BY THE CONSUMER'S WIFE WHO REPORTED THAT HER HUSBAND HAS HAD SEVERAL MORE ATTACKS OF VERY PAIN AND A VERY RED EYEBALL. THE DOCTOR DETERMINED THAT HE HAS IRITIS. HE PRESCRIBED STEROID EYE DROPS.
Patient problems: Excessive Tear Production; Eye Pain; Iritis; Red Eye(s)
MAUDE report 11873949 ↗
Other intraocular lens devices
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens146 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens145 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens144 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens139 reports
- TECNIS SIMPLICITY DIB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens1 recall81 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens129 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens127 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens126 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page