ACRYSOF® SN6AT5 (REF SN6AT5.070)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, 3.00 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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00380652250733), received between May 23, 2023 and May 23, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Markings/Labelling Problem” (1 report).
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
- Device Markings/Labelling Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 23, 2023Device Markings/Labelling Problem; Device Markings/Labelling Problem
A PHARMACIST REPORTED FOLLOWING THE INTRAOCULAR LENS IMPLANTATION INSUFFICIENT INFORMATION" ON THE PACKAGING OF THE IMPLANT, LEADING TO A TRACEABILITY ERROR. IT APPEARS THAT THE BARCODE ON THE LABEL CONTAINS THE FOLLOWING REFERENCE "SN6AT70D", WHICH CAUSED A SOFTWARE BUG AND RESULTED IN A TRACEABILITY ERROR TO THE PATIENT (TRACEABILITY OF AN SN6AT3 18.5D WHEN THE PATIENT WAS GIVEN AN SN6AT5 7D). ADDITIONAL INFORMATION HAS BEN REQUESTED AND RECEIVED STATING THE EVEN THOUGH THE PATIENT WAS IMPLANTED WITH THE EXPECTED IMPLANT. THE REFERENCE WAS WRONG IN THE BAR CODE OF THE LENS BOX THAT LEAD TO TRACEABILITY ERROR.
Patient problems: Insufficient Information
MAUDE report 16982101 ↗
Other intraocular lens devices
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- 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.
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