Skip to content

TECNIS IOL DFW150 (REF DFW150U090)Recalls & reported problems

Johnson & Johnson Surgical Vision, Inc. · TECNIS SYNERGY TORII SMPCY 09.0D 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 05050474751040), received between Jan 5, 2023 and Jan 5, 2023 — 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

  • Blurred Vision1
  • Halo1

Recent adverse event reports

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

  • InjuryJan 5, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT AN INTRAOCULAR LENS (IOL) WAS EXTRACTED FROM THE PATIENT'S RIGHT EYE. MR PRE-OP: -10.25+0.75X135 20/20-2. MR POST-OP DAY 6: -0.25+0.50X92 20/20. THE PATIENT COMPLAINED OF CONSISTENT FOGGY VISION AND CIRCLES IN VISION. WORSE WITH MORE LIGHTING. NO SURGICAL COMPLICATIONS REPORTED. NO VITRECTOMY WAS REQUIRED. POST OP DROPS GIVEN. CELLS AND FLARE MINIMAL. IRIS TRANS ILLUMINATION DEFECTS PARALLEL. EVERYTHING ELSE WITHIN NORMAL. OPTICAL COHERENCE TOMOGRAPHY (OCT) COMPLETED AND NORMAL. NO OTHER INFORMATION WAS PROVIDED.

    Patient problems: Blurred Vision; Halo

    MAUDE report 16110069 ↗

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.