Skip to content

TECNIS IOL DFW300 (REF DFW300U135)Recalls & reported problems

Johnson & Johnson Surgical Vision, Inc. · TECNIS SYNERGY TORII SMPCY 13.5D CYL3.00 · 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 05050474752313), received between Oct 19, 2022 and Oct 19, 2022 — 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

Recent adverse event reports

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

  • InjuryOct 19, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT AN INTRAOCULAR LENS (IOL) WAS EXPLANTED AS THE PATIENT HAD TROUBLE SEEING DISTANCE AS WELL AS NEAR AND WAS UNHAPPY WITH THE RESULTS. A NON-JOHNSON AND JOHNSON LENS OF +16.5 DIOPTER WAS IMPLANTED IN THE PATIENT¿S LEFT EYE AS THE REPLACEMENT. THE PATIENT¿S SYMPTOMS IMPROVED POST EXPLANT, AND NO INJURY WAS REPORTED. THE DEVICE IS NOT AVAILABLE FOR RETURN. NO FURTHER INFORMATION WAS PROVIDED.

    Patient problems: Blurred Vision

    MAUDE report 15635635 ↗

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.