AcrySof™ IQ PanOptix™ Toric UV IOL TFAT30 (REF TFAT30.330)Recalls & reported problems
Alcon Laboratories, Inc. · AcrySof® IQ PanOptix® Toric Trifocal intraocular lenses (IOLs) are ultraviolet absorbing foldable multifocal IOLs · Class 3 · Implant
All models of AcrySof IQ PanOptix Toric UV IOL (120)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00380652418935), received between Mar 31, 2023 and Mar 31, 2023 — classified as 2 injuries.
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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Blurred Vision2
- Halo2
- Visual Disturbances2
- Visual Impairment2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMar 31, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A NON-HEALTH ARE PROFESSIONAL REPORTED FOLLOWING THE INTRAOCULAR LENS IMPLANTATION THE PATIENT WAS EXTREMELY UNHAPPY AND DISSATISFIED AND COMPLAINTS OF GLARES, HALOS AND STATES HAS LOST DEPTH PERCEPTION AND SAYS EVERYTHING IS ¿A HAZE AND A FOG." ADDITIONAL INFORMATION WAS REQUESTED AND RECEIVED STATING THE SYMPTOMS ARE STILL ONGOING AND THE PATIENT STILL REMAINS UNHAPPY AND DISSATISFIED. THERE WAS HARM TO THE PATIENT I.E. SIGNIFICANT VISUAL DISCOMFORT. THERE ARE TWO MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS PATIENT. THIS REPORT IS FOR THE RIGHT EYE.
Patient problems: Blurred Vision; Halo; Visual Disturbances; Visual Impairment
MAUDE report 16654685 ↗InjuryMar 31, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A NON-HEALTH ARE PROFESSIONAL REPORTED FOLLOWING THE INTRAOCULAR LENS IMPLANTATION THE PATIENT WAS EXTREMELY UNHAPPY AND DISSATISFIED AND COMPLAINTS OF GLARES AND HALO AND STATES HAS LOST DEPTH PERCEPTION AND SAYS EVERYTHING IS ¿A HAZE AND A FOG." ADDITIONAL INFORMATION WAS REQUESTED AND RECEIVED STATING THE SYMPTOMS ARE STILL ONGOING AND THE PATIENT STILL REMAINS UNHAPPY AD DISSATISFIED. THERE WAS HARM TO THE PATIENT I.E. SIGNIFICANT VISUAL DISCOMFORT. THERE ARE TWO MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS PATIENT. THIS REPORT IS FOR THE LEFT EYE.
Patient problems: Blurred Vision; Halo; Visual Disturbances; Visual Impairment
MAUDE report 16654614 ↗
Other Lens, multifocal intraocular devices
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular144 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular1 recall66 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular113 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular112 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular110 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular107 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular104 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular93 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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