TECNIS IOL ZXT225 (REF ZXT225U050)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TECNIS SYMFONY TORIC ERV 05.0D CYL2.25 · Class 3 · Implant
All models of TECNIS IOL (1344)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 05050474605497), received between Aug 1, 2019 and Aug 1, 2019 — classified as 1 injury.
The most frequently reported specific device problem is “Unintended Movement” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Unintended Movement1
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.
InjuryAug 1, 2019Unintended Movement; Unintended Movement
WHILE DOING A FOLLOW-UP ON AN EVENT, NEW INFORMATION WAS RECEIVED THAT ORIGINAL INTRAOCULAR LENS (IOL) A ZXT225 WHICH THE AR40M IOL WAS PIGGYBACKING ON ROTATED 40 DEGREES FROM ITS ORIGINAL LOCATION. THERE WAS A MYOPIC MISS. IT WAS LEARNT THAT THE DOCTOR REMOVED THE PIGGYBACK LENS AND REPOSITIONED THE ZXT225 BOTH ON (B)(6) 2019 AND PATIENT IS NOW HAPPIER. THE EXPLANT EVENT FOR THE PIGGYBACK IOL IS CAPTURED IN A SEPARATE REPORT.
Patient problems: No Code Available
MAUDE report 8853418 ↗
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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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