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TECNIS IOL DFR00V (REF DFR00VU270)Recalls & reported problems

Johnson & Johnson Surgical Vision, Inc. · TECNIS SYNERGY SIMPLICITY 27.0D · 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 05050474750814), received between May 12, 2022 and May 12, 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
  • Halo1

Recent adverse event reports

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

  • InjuryMay 12, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT THE PRELOADED INTRAOCULAR LENS (IOL) WAS EXPLANTED FROM THE LEFT EYE AS PATIENT COMPLAINED OF HALOS AT NIGHT AND BLURRY DISTANCE VISION. ANOTHER COMPETITOR LENS OF SMALLER DIOPTER (26.5D) WAS USED AS THE REPLACEMENT IOL. THERE WAS NO OTHER INJURY REPORTED. NO OTHER INTERVENTION WAS REQUIRED. THE PATIENT WAS DOING GOOD POST OPERATION. NO FURTHER INFORMATION WAS PROVIDED.

    Patient problems: Blurred Vision; Halo

    MAUDE report 14378849 ↗

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.