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TECNIS IOL ZMB00 (REF ZMB00U0090)Recalls & reported problems

Johnson & Johnson Surgical Vision, Inc. · TECNIS MF 1- PIECE 6.0MM 9.0 US · 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 05050474535404), received between Nov 4, 2019 and Nov 4, 2019 — 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

  • No Code Available1

Recent adverse event reports

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

  • InjuryNov 4, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT SURGEON WILL REPLACE THE CURRENT TECNIS MULTIFOCAL INTRAOCULAR LENS FROM PATIENT¿S LEFT EYE WITH A DIFFERENT POWER TECNIS MULTIFOCAL INTRAOCULAR LENS BECAUSE OF PATIENT EXPERIENCING REFRACTIVE ERROR. REPORTEDLY DATE FOR EXPLANT HAS NOT BEEN SCHEDULED. NO FURTHER INFORMATION PROVIDED.

    Patient problems: No Code Available

    MAUDE report 9273203 ↗

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.