ACRYSOF® SN60AT (REF SN60AT.330)Recalls & reported problems
Alcon Laboratories, Inc. · AcrySof(R) Natural SINGLE-PIECE ACRYLICFOLDABLE IOL, UV WITH BLUE LIGHT FILTER,POSTERIOR CHAMBER LENS (IOL/PC), 13.0mm LENGTH,6.0mm BICONVEX OPTIC, PLANAR HAPTICS. · Class 3 · Implant
All models of ACRYSOF (353)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00380650130532), received between Apr 1, 2022 and Nov 12, 2024 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Defective Device” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Defective Device2
- Break1
- Defective Component1
- Failure to Advance1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
- Insufficient Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 12, 2024Defective Component; Defective Device; Defective Component; Defective Device
A SURGEON REPORTED DURING INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, WHILE PREPARING THE IOL FOR IMPLANTATION, THE PLUNGER PASSED OVER THE LENS AND PINCHED THE POSTERIOR HAPTIC UPON EXIT. DUE TO THE UNAVAILABILITY OF AN IOL WITH THIS DIOPTER, THE PATIENT WAS DISCHARGED WITHOUT THE IOL IMPLANTATION (APHAKIC EYE), AND A SIMILAR IOL IMPLANTATION WAS SCHEDULED SOON. NO PATIENT HARM. ADDITIONAL INFORMATION HAS BEEN RECEIVED STATING NO PATIENT CONTACT WITH COMPANY PRODUCT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20664437 ↗MalfunctionMar 7, 2023Break; Failure to Advance; Break; Failure to Advance
A RISK MANAGER REPORTED THAT DURING A CATARACT EXTRACTION WITH AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, LENS BECAME STUCK IN THE INCISION. HAPTIC BROKEN OFF OF THE LENS UPON RETRIEVING THE LENS. THERE WAS NO SERIOUS HARM REPORTED. UNEXPECTED OR PROLONGED CARE WAS NOT REQUIRED. ADDITIONAL INFORMATION WAS REQUESTED, BUT FURTHER NO INFORMATION WAS AVAILABLE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16493730 ↗MalfunctionApr 1, 2022Defective Device; Defective Device
A FACILITY REPRESENTATIVE REPORTED VIA REPLY CARD WITH AN DESCRIPTION OF AN DEFECTIVE INTRAOCULAR LENS AND NOT USED THE IOL. ADDITIONAL INFORMATION HAS BEEN REQUESTED.
Patient problems: Insufficient Information
MAUDE report 13974423 ↗
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.
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