TECNIS IOL ZXT150 (REF ZXT150U130)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TECNIS SYMFONY TORIC ERV 13.0D CYL1.50 · Class 3 · Implant
All models of TECNIS IOL (1344)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 05050474605060), received between Feb 19, 2018 and May 16, 2018 — classified as 2 injuries.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- No Code Available2
- Visual Disturbances1
- Visual Impairment1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 16, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE SURGEON WAS PLANNING TO EXPLANT A TECNIS SYMFONY TORIC MULTIFOCAL INTRAOCULAR LENS (MODEL ZXT150, +13.0 DIOPTER) FROM PATIENT¿S RIGHT EYE IN SECONDARY PROCEDURE BECAUSE OF PATIENT EXPERIENCING CLOUDY VISION, TROUBLE WITH DISTANCE AND NEAR VISION. AT THE TIME OF THIS REPORT, THE LENS HAS NOT YET BEEN EXPLANTED. NO FURTHER INFORMATION PROVIDED.
Patient problems: No Code Available; Visual Disturbances; Visual Impairment
MAUDE report 7521063 ↗InjuryFeb 19, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A TECNIS SYMFONY INTRAOCULAR LENS (MODEL ZXT150, +13.0 DIOPTER) WAS EXPLANTED IN A SECONDARY PROCEDURE FROM PATIENT'S LEFT EYE BECAUSE OF PATIENT'S NON-SPECIFIED DYSPHOTOPSIA. A NON-AMO INTRAOCULAR LENS WITH +14.5 DIOPTER WAS IMPLANTED AS REPLACEMENT LENS FOR THE PATIENT. THERE WERE NO COMPLICATIONS REPORTED AND THE PATIENT WAS DOING FINE POST OP. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: No Code Available
MAUDE report 7281518 ↗
Other Extended depth of focus intraocular lens devices
- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens101 reports
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- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens93 reports
- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens89 reports
- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens87 reports
- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens75 reports
- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens73 reports
- TECNIS IOL ZXR00Johnson & Johnson Surgical Vision, Inc. · Extended depth of focus intraocular lens71 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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