TECNIS IOL DXW150 (REF DXW150U255)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TEC SYMF TOR II OB SMPCY 25.5 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 05050474763081), received between May 20, 2026 and May 20, 2026 — 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.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Visual Impairment1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 20, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT HAD IMPLANTATION OF A SINGLE PIECE PRELOADED TORIC INTRAOCULAR LENS (IOL) IN THE RIGHT EYE. IT WAS STATED THE PATIENT HAVING DIFFICULTY DRIVING AS THEY WERE UNABLE TO DRIVE SAFELY DUE TO SYMPTOMS. THE PATIENT WAS OVERCORRECTED. PRE OPERATIVE REFRACTION: -2.75 +2.50 ×099 AND BEST SPECTACLE CORRECTED VISUAL ACUITY (BSCVA) OF 20/25. POST OPERATIVE REFRACTION: +1.25 +2.00 ×165 WITH BSCVA OF 20/30 . THE INITIAL TARGET REFRACTION WAS PLANO SPHERE. IOL WAS EXPLANTED AND REPLACED IN A SECONDARY SURGICAL INTERVENTION BY A SINGLE PIECE TORIC MONOFOCAL INTRAOCULAR LENS (IOL) OF 24.0 DIOPTER. FOLLOWING THE LENS EXCHANGE, THE POST-OPERATIVE REFRACTION WAS -0.75 +2.00 ×158, AND THE PATIENT REPORTED IMPROVED SUBJECTIVE VISION. NO FURTHER INFORMATION WAS PROVIDED. PRODUCT IS NOT AVAILABLE FOR RETURN.
Patient problems: Visual Impairment
MAUDE report 25236604 ↗
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- 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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