TECNIS IOL DXW150 (REF DXW150U115)Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 05050474762800), received between Sep 28, 2023 and Jun 4, 2025 — classified as 3 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.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• InjuryJun 4, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A TORIC INTRAOCULAR LENS (IOL) WAS EXPLANTED FROM A PATIENT'S LEFT EYE DUE TO PATIENT BEING UNABLE TO TOLERATE THE LENS. THE REPLACEMENT IOL WAS OF A DIFFERENT MODEL AND HIGHER DIOPTER (MODEL: DIU150,12.0D). NO PATIENT INJURY OR COMPLICATION REPORTED. THE DEVICE IS NOT AVAILABLE FOR RETURN AS IT WAS DISCARDED BY THE ACCOUNT. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: Visual Disturbances

  MAUDE report 22146793 ↗
• InjuryFeb 1, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT THE PATIENT HAD SLIGHT BLURRINESS AFTER IMPLANTING TECNIS SYMPHONY TORIC INTRAOCULAR LENS (IOL). PHYSICIAN WAS GIVING HER TIME TO HEEL. ADDITIONAL INFORMATION RECEIVED CONFIRMED THAT THE PATIENT DOES NOT HAVE ANY DEBILITATION CONDITION DUE TO BLURRINESS. NO FURTHER MEDICAL INTERVENTION WAS REQUIRED. CURRENTLY PATIENTS' VISION IS SLIGHTLY BLURRY. DOCTOR PLANS FOR LASIK ENHANCEMENT FUTURE VISIT. THROUGH FOLLOW UP, IT WAS LEARNT THAT AT THE PRESENT MOMENT PATIENT HAS NOT HAD LASIK ENHANCEMENT, HOWEVER PATIENT IS SCHEDULED FOR A FOLLOW UP APPOINTMENT 10/5/23. FURTHER FOLLOW UP INFORMATION REVEALED THAT PATIENT HAD A FOLLOW UP APPOINTMENT ON 10/16/2023. DOCTOR CONTINUES TO MONITOR THE PATIENT, CURRENTLY NO FURTHER TREATMENT IS NEEDED. ADDITIONAL INFORMATION RECEIVED STATED THAT THE ORIGINAL LENS WAS EXPLANTED. DOCTOR DECIDED TO DO THE EXPLANT ON (B)(6) 2023. THERE WAS NO PATIENT INJURY. NO OTHER MEDICAL OR SURGICAL INTERVENTION REQUIRED. THE ORIGINAL LENS WAS REPLACED WITH ZCB00 11.5 DIOPTER LENS. PATIENTS OUTCOME WAS REPORTED AS PATIENT MUST IMPROVE AND HER VISION WAS MUCH BETTER AND HER LENS WAS IN A GOOD POSITION ON ONE DAY POST EXPLANT. NO FURTHER INFO

  Patient problems: Blurred Vision

  MAUDE report 18624154 ↗
• InjurySep 28, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  A PLANNED EXPLANT OF A TORIC INTRAOCULAR LENS (IOL) WAS REPORTED AS THE PATIENT COMPLAINED ABOUT THEIR VISION. ADDITIONAL INFORMATION INDICATED THAT THE PATIENT COMPLAINED OF HAVING BLURRY VISION AND THE IOL WAS EXPLANTED FROM THE PATIENT'S RIGHT EYE AS SCHEDULED ON (B)(6) 2023. ANOTHER TORIC LENS OF DIFFERENT MODEL AND DIOPTER (DIU150, 12.5 D) WAS USED AS A REPLACEMENT. THE PATIENT IS STABLE POST-EXPLANT AND NO INJURY REPORTED. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: Blurred Vision

  MAUDE report 17840401 ↗