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TECNIS IOL ZLU150 (REF ZLU150U220)Recalls & reported problems

Johnson & Johnson Surgical Vision, Inc. · TECNIS TORIC LOW ADD 1-PC 22.0D CYL1.50 · 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 05050474689404), received between Mar 31, 2021 and Mar 31, 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Visual Impairment1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 31, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT AN INTRAOCULAR LENS (IOL) WAS EXCHANGED. NO ADDITIONAL INFORMATION WAS PROVIDED. THROUGH FOLLOW-UP, IT WAS LEARNED THAT THE LENS WAS EXPLANTED DUE TO THE PATIENT EXPERIENCING A HYPEROPIC OUTCOME. THE LENS WAS DISCARDED. THERE WAS NO VITRECTOMY, INCISION ENLARGEMENT, OR SUTURES REQUIRED. ANOTHER JOHNSON & JOHNSON LENS (SAME MODEL AND HIGHER DIOPTER) WAS SUCCESSFULLY IMPLANTED AS A REPLACEMENT. NO ADDITIONAL INFORMATION WILL BE AVAILABLE.

    Patient problems: Visual Impairment

    MAUDE report 11599771 ↗

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.