TECNIS IOL DXW150 (REF DXW150U180)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TEC SYMF TOR II OB SMPCY 18.0 CYL1.50 · Class 3 · Implant
All models of TECNIS IOL (1344)
Data updated Oct 18, 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 05050474762930), received between Jan 6, 2023 and Sep 13, 2024 — classified as 2 injuries.
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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem2
Patient problems
- Blurred Vision1
- Halo1
- Visual Disturbances1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjurySep 13, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT THE PRELOADED INTRAOCULAR LENS (IOL) WAS EXPLANTED FROM PATIENT LEFT EYE IN A SECONDARY PROCEDURE. THE PATIENT REPORTED OF DISTANCE VISUAL ACUITY AND NEAR VISUAL ACUITY WAS VERY BLURRY. VISUAL ACUITY WAS UNBALANCED WITH VA OF 20/25 IN LEFT EYE. THE LENS WAS REPLACED WITH A DIB00 LENS AND THE PATIENT FEELS GOOD WITH THE REPLACED LENS. THERE WAS NO PATIENT INJURY AND THERE WAS NO MEDICAL/SURGICAL INTERVENTION REQUIRED. THE PATIENT HAD FULLY RECOVERED. NO OTHER INFORMATION IS AVAILABLE.
Patient problems: Blurred Vision
MAUDE report 20216550 ↗InjuryJan 6, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT AN INTRAOCULAR LENS (IOL) WAS EXPLANTED FROM THE PATIENT'S RIGHT EYE DUE TO EXCESSIVE GLARE AND HALO, DYPHOTOPSIA AND AS THE PATIENT WAS NOT HAPPY WITH VISUAL OUTCOME. THE PATIENT'S DAILY ACTIVITIES WERE SIGNIFICANTLY AFFECTED. REPLACEMENT IOL AND IS DIU150 17.5 DIOPTER. THERE WAS NO VITRECTOMY PERFORMED, NO SUTURES REQUIRED AND NO DELAY IN PROCEDURE REPORTED. THE PATIENT IS VERY HAPPY WITH HER VISION POST EXPLANT. NO OTHER INFORMATION WAS PROVIDED.
Patient problems: Halo; Visual Disturbances
MAUDE report 16118699 ↗
Other intraocular lens devices
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens146 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens145 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens144 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens139 reports
- TECNIS SIMPLICITY DIB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens1 recall81 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens129 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens127 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens126 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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