TECNIS IOL ZLU150 (REF ZLU150U235)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TECNIS TORIC LOW ADD 1-PC 23.5D 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
- 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 05050474689435), received between Jul 12, 2022 and Jul 12, 2022 — classified as 1 injury.
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
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Blurred Vision1
- Dry Eye(s)1
- Foreign Body Sensation in Eye1
- Inflammation1
- Insufficient Information1
- Vitreous Floaters1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 12, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PATIENT EXPERIENCED BLURRY VISION THE SECOND DAY AFTER THE INTRAOCULAR LENS (IOL) WAS IMPLANTED IN THE LEFT EYE. THE PATIENT DESCRIBED THE VISION AS A ¿GEL¿ OVER THE EYE. THE PATIENT FEELS LIKE THE EYE AND PUPIL ARE SWOLLEN. THE PATIENT WAS TOLD THAT ¿IT LOOKS VISIBLY DIFFERENT; IT LOOKS LIKE IT IS WIDER AND ONE CAN SEE MORE OF THE PUPIL.¿ THE PATIENT BELIEVES THAT THE ISSUE IS PUTTING STRAIN ON THE RIGHT EYE TO COMPENSATE. THE PATIENT HAS MENTIONED IT TO THE DOCTOR SEVERAL TIMES AND WAS DIAGNOSED AND TREATED FOR DRY EYE. THE PATIENT WAS PRESCRIBED RESTASIS, WHICH THE PATIENT REPORTED DID NOT WORK. YTTRIUM ALUMINUM GARNET (YAG) WAS PERFORMED FOR ¿SCAR TISSUE¿ ON (B)(6) 2022 AND (B)(6) 2022 WITH "NEGATIVE RESULT." THE PATIENT IS NOW BEING TREATED FOR DRY EYE AGAIN. THE PATIENT REPORTED VISION IS WORSE THAN BEFORE. THE ISSUE IS NOT CAUSING ANY DISABILITY OTHER THAN IT BEING EXHAUSTING. THE PATIENT DOES NOT WEAR GLASSES OR CONTACTS, BUT OCCASIONALLY WEAR "CHEATERS" GLASSES DUE TO "TIRED EYES." THE PATIENT WAS OFFERED TO BE FIT FOR GLASSES, BUT THE PATIENT DISAGREES WITH THAT OPTION. THE PATIENT HAS NO OTHER HEALTH CONDITIONS. THERE WERE NO OTHER SURGICAL INTER
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Blurred Vision; Dry Eye(s); Foreign Body Sensation in Eye; Inflammation; Insufficient Information; Vitreous Floaters
MAUDE report 14991365 ↗
Other Lens, multifocal intraocular devices
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular144 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular1 recall66 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular113 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular112 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular110 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular107 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular104 reports
- Clareon™ CNA0T0Alcon Laboratories, Inc. · Lens, multifocal intraocular93 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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