TECNIS IOL DXW225 (REF DXW225U275)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TEC SYMF TOR II OB SMPCY 27.5D CYL2.25 · 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 05050474764309), received between Jun 30, 2023 and Jun 30, 2023 — 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
- Halo1
- Visual Disturbances1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 30, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT IS REPORTED THAT DXW225 INTRAOCULAR LENS WAS EXPLANTED FROM PATIENT'S RIGHT EYE DUE TO GLARE AND HALO. DXW225 LENS WAS REPLACED WITH DIU225 LENS SUCCESSFULLY. ADDITIONAL INFORMATION RECEIVED REVEALED THAT IMMEDIATELY POSTOP, THE PATIENT NOTED SEVERE GLARE WHICH MADE IT DIFFICULT TO DRIVE AT NIGHT. IT WAS CONFIRMED THAT THE LENS WAS REMOVED AND REPLACED IN A SECONDARY PROCEDURE. THERE WAS NO PATIENT INJURY AND MEDICAL OR SURGICAL INTERVENTIONS WERE NOT REQUIRED. POST SURGERY, THE PATIENT'S UCVA WAS 20/25, MR(MEDIAL RECTUS) WAS -0.75 D SPHERE. IT WAS INFORMED THAT PUTTING THE CORRECTION IN FRONT OF HIM DID NOT IMPROVE THE GLARE. THE DXW225 LENS WAS NOT BEING RETURNED AS IT WAS BISECTED AND NOT SAVED. NO FURTHER INFORMATION WAS PROVIDED.
Patient problems: Halo; Visual Disturbances
MAUDE report 17240741 ↗
Other intraocular lens devices
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- 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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