TECNIS IOL ZXT150 (REF ZXT150U070)Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 05050474604940), received between Jun 28, 2017 and Mar 29, 2019 — 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. How this data works · Data updated Oct 13, 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.

• InjuryMar 29, 2019Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A PATIENT HAD BILATERAL SYMFONY TORIC IMPLANTS IN 2017. THE PATIENT THEN DEVELOPED GLARE AND JUST WANTS BOTH LENSES OUT. THE DOCTOR PLANNED ON PUTTING IN A STANDARD TORIC LENS BUT ADVISED THE PATIENT THAT IF THERE IS ANY ISSUE WILL GO WITH A STANDARD LENS. THE ZXT150 SYMFONY TORIC WAS REMOVED FROM HER LEFT EYE (OS) ON (B)(6) 2019. THE NEW INTRAOCULAR LENS (IOL) WAS A MODEL ZCT225, +8.00. NO VITRECTOMY OR SUTURES AND NO POST-OP INJURIES. NO OTHER INFORMATION WAS PROVIDED. THIS MDR REPORT PERTAINS TO THE LEFT EYE (OS). A SEPARATE REPORT WILL BE SUBMITTED FOR THE RIGHT EYE (OD).

  Patient problems: Halo; No Code Available

  MAUDE report 8466621 ↗
• InjuryJun 28, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT A ZXT150 7.0 DIOPTER INTRAOCULAR LENS WAS IMPLANTED IN THE PATIENT'S OPERATIVE EYE. IT WAS LATER EXPLANTED DUE TO RESIDUAL MYOPIA. NO ADDITIONAL INFORMATION WAS PROVIDED.

  Patient problems: No Code Available

  MAUDE report 7644814 ↗
• InjuryJun 28, 2017Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  INITIALLY, IT WAS REPORTED A PATIENT HAD ISSUES WITH HER VISION AFTER IMPLANTATION OF A ZXT150 7.0 DIOPTER INTRAOCULAR LENS (IOL) IN HER LEFT EYE AT AXIS 75 DEGREES. IMPLANT TOOK PLACE ON (B)(6) 2016. PATIENT CLAIMS THAT SHE COULD NOT SEE NEAR HER PHONE AND (B)(6). FURTHERMORE, SHE ADDED THAT AT NIGHT IT LOOKS LIKE SHE'S SEEING FIREWORKS. BUT HER DISTANCE VISION IS WELL. THE CLINIC CONFIRMED THAT THE LENS IMPLANTED IN THE PATIENT HAD NO ISSUES AND SURGERY WENT WELL. THE PATIENT FOLLOWED UP WITH THE CLINIC AND PATIENT IS STILL COMPLAINING BUT DOCTOR DOESN'T KNOW WHY, AS HER VISUAL ACUITY (VA) IS 20/20, UNCOMPLICATED S/P CATARACT AND PERFECT DISTANCE OUTCOME. SHE COMPLAINS OF STARBURSTS BUT DOCTOR THINKS THAT THEY SHOULD GO AWAY IN TIME. THERE WAS PLAN TO EXPLANT. ON (B)(4) 2017, AMO WAS NOTIFIED THAT THE PATIENT IS NOW A CANDIDATE FOR A LENS EXCHANGE AS SHE IS EXTREMELY UNHAPPY WITH THE LENS. PATIENT IS EXPERIENCING A SIGNIFICANT AMOUNT OF NIGHT TIME GLARE. PATIENT IS SCHEDULED TO HAVE THE LENS EXPLANTED. NO FURTHER INFORMATION WAS PROVIDED.

  Patient problems: Halo; No Code Available

  MAUDE report 6675656 ↗