TECNIS IOL ZCT150 (REF ZCT150U100)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TECNIS TORIC 1-PIECE 6.0MM 10.0D 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
- 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 05050474551947), received between Nov 16, 2020 and Nov 16, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
- Device Dislodged or Dislocated1
Patient problems
- Blurred Vision1
- No Code Available1
- Vitrectomy1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 16, 2020Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT A MODEL ZCT150 INTRAOCULAR LENS (IOL) WAS REPOSITIONED DUE TO PSEUDOPHAKODONESIS. MEDICAL/SURGICAL INTERVENTIONS THAT WERE PERFORMED ARE IOL REPOSITIONING, PARS PLANA VITRECTOMY (PPV), USE OF CAPSULAR RETRACTORS, CAPSULAR TENSION SET RING, AND PLACEMENT OF 2 CAPSULE TENSION SEGMENTS SUTURED IN PLACE. PATIENT IS HAPPY WITH THE VISION AND IOL IS IN GOOD POSITION. ADDITIONAL DETAILS RECEIVED STATES THAT THERE IS NO "DEGREE" OF ROTATION OF THE IOL AND THE REASON FOR THE REPOSITIONING WAS PSEUDOPHAKODONESIS - WHICH IS MOVEMENT/JIGGLING OF THE IOL. PATIENT'S FIRST COMPLAINT OF BLURRY VISON IN THE RIGHT EYE (OD) WAS ON (B)(6) 2019. VISION WAS 20/25+2 WITH CORRECTION. DOCTOR DOCUMENTED PSEUDOPHAKODONESIS THEN ADVISED TO OBSERVE. PATIENT RETURNED ON (B)(6) 2020 WITH THE SAME COMPLAINT OF BLURRY VISION - 20/25 WITH CORRECTION IN THE RIGHT EYE AND ADVISED TO OBSERVE. PATIENT RETURNED AGAIN ON (B)(6) 2020 WITH COMPLAINT OF BLURRY VISION - 20/30 WITH CORRECTION THEN DOCTOR ADVISED SURGERY TO LASSO THE IOL. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Blurred Vision; No Code Available; Vitrectomy
MAUDE report 10849062 ↗
Other LENS, INTRAOCULAR, TORIC OPTICS devices
- TECNIS IOL ZCT150Johnson & Johnson Surgical Vision, Inc. · LENS, INTRAOCULAR, TORIC OPTICS1 recall7 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS43 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS36 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS32 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS30 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS29 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS21 reports
- TECNIS IOL DIU150Johnson & Johnson Surgical Vision, Inc. · LENS, INTRAOCULAR, TORIC OPTICS19 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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