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AcrySof® IQ PanOptix® Trifocal IOL TFNT00 (REF TFNT00.105)Recalls & reported problems

Alcon Laboratories, Inc. · AcrySof® IQ PanOptix® Trifocal intraocular lenses is an ultraviolet absorbing and blue light filtering foldable multifocal IOL · Class 3 · Implant

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 00380652392747), received between Jul 24, 2023 and Jul 24, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Defective Device” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Defective Device1

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.

  • InjuryJul 24, 2023Defective Device; Defective Device

    A NURSE REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, THE HAPTIC OF THE IOL WAS FOUND TO BE POSITIONED ABOVE THE ANTERIOR CAPSULE, EXTENDING BEYOND THE CCC MARGIN, AND THE DISTAL END OF THE HAPTIC WAS DISTORTED. THEREFORE, A LENS EXCHANGE WAS PERFORMED IN A SECONDARY PROCEDURE.

    Patient problems: Insufficient Information

    MAUDE report 17378575 ↗

Other Lens, multifocal intraocular devices

All Lens, multifocal intraocular devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.