TECNIS IOL ZCT150 (REF ZCT150U140)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TECNIS TORIC 1-PIECE 6.0MM 14.0D 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05050474552029), received between Nov 19, 2021 and Nov 19, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Contamination” (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
- Contamination1
- Device Contaminated During Manufacture or Shipping1
Patient problems
- Blurred Vision1
- Inflammation1
- Visual Disturbances1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryNov 19, 2021Contamination; Device Contaminated During Manufacture or Shipping; Contamination; Device Contaminated During Manufacture or Shipping
IT WAS REPORTED THAT A PATIENT COMPLAINED ABOUT THEIR VISION AND THE DOCTOR FOUND PLASTIC PIECES BILATERALLY ON EACH INTRAOCULAR LENS (IOL). THE LENSES HAVE NOT BEEN EXPLANTED BUT THE DOCTOR DID ATTEMPT TO REMOVE THE FOREIGN BODY. A MICROORGANISM CULTURE FOUND NOTHING. THE DOCTOR SAW THE PATIENT IN (B)(6) 2021 WITH COMPLAINTS OF PHOTOPHOBIA, DECREASED VISION IN BOTH EYES WHICH IS THE FIRST RECORD OF ANTERIOR SEGMENT FOREIGN BODY. REPORTEDLY, THIS ISSUE WAS NOT NOTED IN POST OPERATIVE VISITS OR RETINA VISIT AT OUTSIDE OFFICES. INITIAL MEDICAL TREATMENT WITH AGGRESSIVE TOPICAL STEROIDS AND NSAIDS WAS SUCCESSFUL, INFLAMMATION AND VISION BOTH IMPROVED HOWEVER BOTH WORSENED AFTER TAPERING OF DROPS. THE PATIENT WENT THROUGH THE CYCLE A FEW TIMES WITHOUT SUCCESS OF TAPERING OFF DROPS. THROUGH THREE (3) WEEKS TAPERING DROPS, THE VISION REMAINED 20/40 BEST CORRECTED VISUAL ACUITY (BCVA). THE APPEARANCE OF FOREIGN BODY WAS COMPLETELY UNCHANGED AFTER SEVERAL MONTHS. THE DOCTOR DECIDED TO GO FOR SURGERY ON (B)(6) 2021 FOR FOREIGN BODY REMOVAL AND IT DID NOT BEHAVE AS EXPECTED. THE DOCTOR WAS UNABLE TO GET ENOUGH TO SEND FOR PATHOLOGY BUT THEY CULTURED A FRAGMENT AND THE AC WHICH WERE NEGATIVE
Patient problems: Blurred Vision; Inflammation; Visual Disturbances
MAUDE report 12844662 ↗
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.
How reports and recalls are matched · Editorial policy · Report an error on this page