TECNIS IOL ZCT150 (REF ZCT150U295)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TECNIS TORIC 1-PIECE 6.0MM 29.5D 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 05050474552333), received between Jul 19, 2018 and May 31, 2019 — classified as 2 injuries.
The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (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
- Adverse Event Without Identified Device or Use Problem1
- Inadequacy of Device Shape and/or Size1
Patient problems
- No Code Available2
- Blurred Vision1
- Headache1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 31, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE INTRAOCULAR LENS (IOL) WAS EXPLANTED AND REPLACED WITH ANOTHER IOL OF THE SAME MODEL BUT LOWER DIOPTER. ADDITIONAL INFORMATION RECEIVED REVEALED THE PATIENT REPORTED HAVING BLURRY VISION, WAS UNABLE TO TOLERATE MONOVISION, HEADACHES AND UNABLE TO DRIVE AT NIGHT. THERE WAS NO ADDITIONAL SURGICAL OR MEDICAL INTERVENTION PERFORMED. ALL SYMPTOMS HAVE DISAPPEARED AND PATIENT IS 20/20 UNCORRECTED AT DISTANCE. NO ADDITIONAL INFORMATION WAS RECEIVED.
Patient problems: Blurred Vision; Headache; No Code Available
MAUDE report 8657048 ↗InjuryJul 19, 2018Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size
IT WAS REPORTED THAT THE INTRAOCULAR LENS ZCT150 (DIOPTER UNKNOWN) WAS IMPLANTED IN THE RIGHT EYE (OD) OF THE PATIENT ON (B)(6) 2018. THE PATIENT IS POST RADIAL KERATOTOMY (RK) WITH A THREE (3) DIOPTER REFRACTIVE SURPRISE. REPORTEDLY, THE LENS WAS EXPLANTED ON (B)(6) 2018, AND REPLACED WITH ANOTHER LENS (SAME MODEL, +26.5 DIOPTER). AT 1-MONTH POST-OP THE PATIENT UNCORRECTED VISION WAS 20/25. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: No Code Available
MAUDE report 7705338 ↗
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