TECNIS IOL DXW150 (REF DXW150U185)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TEC SYMF TOR II OB SMPCY 18.5 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 05050474762947), received between Feb 6, 2026 and Feb 6, 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 Disturbances1
- Visual Impairment1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 6, 2026Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT PATIENT HAD REFRACTIVE LENS EXCHANGE (RLE) IN RIGHT EYE. THE DIRECTIONS FOR USE WERE FOLLOWED. PATIENT PRESENTED POST OP WITH POOR TOLERANCE OF THE MULTIFOCAL LENS AND IT WAS IDENTIFIED THAT PATIENT WAS UNDER-CORRECTED. NO UNPLANNED INCISION ENLARGEMENT, VITRECTOMY, OR SUTURES WERE REQUIRED. THERE WAS NO DELAY IN THE PROCEDURE AND NO MEDICATION OUTSIDE OF STANDARD CARE. THE PATIENT¿S STATUS IS TEMPORARILY IMPAIRED. PATIENT PREOPERATIVELY BEST CORRECTED VISUAL ACUITY (BCVA) FOR BOTH EYES: 20/20 REFRACTION : -0.25 -1.50 × 70 POST-OPERATIVELY: 20/40 BCVA THE REPLACEMENT LENSES WERE JOHNSON & JOHNSON LENS: ZCU150 +19.0 THE INTENDED TARGET REFRACTION WAS PLANO.
Patient problems: Visual Disturbances; Visual Impairment
MAUDE report 24284575 ↗
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- 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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