Skip to content

TECNIS IOL DFW150 (REF DFW150U135)Recalls & reported problems

Johnson & Johnson Surgical Vision, Inc. · TECNIS SYNERGY TORII SMPCY 13.5D CYL1.50 · Class 3 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05050474751132), received between Oct 6, 2022 and Oct 6, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Advance” (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

  • Failure to Advance1
  • Mechanical Problem1
  • Scratched Material1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionOct 6, 2022Mechanical Problem; Failure to Advance; Scratched Material; Mechanical Problem; Failure to Advance; Scratched Material

    HOLD FOR TA 12/21 IT WAS REPORTED THAT THE PRELOADED INTRAOCULAR LENS (IOL) PUSHER WENT UNDER THE LENS WHEN PROGRESSING THE LENS. THE LENS WAS POSSIBLY SCRATCHED AND COULD NOT BE PROGRESSED. THERE WAS NO PATIENT CONTACT WITH PATIENT'S LEFT EYE AND THE EVENT WAS OBSERVED DURING HANDLING OF THE DEVICE. THE PATIENT HAS RECOVERED. NO OTHER INFORMATION WAS PROVIDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15556780 ↗

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.