FDA Adverse Event Injury Summary report: N

TECNIS IOL

MDR report key: 21867570 · Received April 18, 2025

Report

Report Number
3012236936-2025-000107
Event Type
Injury
Date Received
April 18, 2025
Date of Event
March 25, 2025
Report Date
April 18, 2025
Manufacturer
AMO PUERTO RICO MFG. INC.
Product Code
MFK
UDI-DI
05050474715776
PMA / PMN Number
P980040
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

SECTION H3: OTHER 81: THE DEVICE WAS NOT RETURNED FOR EVALUATION. THEREFORE, A FAILURE ANALYSIS OF THE COMPLAINT DEVICE CANNOT BE COMPLETED. A REVIEW OF THE DEVICE HISTORY RECORD AND COMPLAINT TRENDING FOR THIS DEVICE WILL BE PERFORMED. UPON COMPLETION OF THE REVIEW, IF THERE IS ANY FURTHER RELEVANT INFORMATION A SUPPLEMENTAL MEDWATCH WILL BE FILED. ALL PERTINENT INFORMATION AVAILABLE TO JOHNSON & JOHNSON SURGICAL VISION, INC. HAS BEEN SUBMITTED.

Description of Event or Problem · 0

IT WAS REPORTED THAT AFTER THE IMPLANTATION OF TORIC MULTIFOCAL INTRAOCULAR LENS (IOL), THE PATIENT'S VISION DID NOT SHOW FAR VISUAL ACUITY. UPON CHECKING, A DIOPTER ERROR WAS IDENTIFIED, SO AN EXCHANGE SURGERY WAS PERFORMED. REPORTEDLY, ZFW150 18.5 DIOPTER LENS WAS REPLACED WITH ZFW150 18 DIOPTER LENS. THROUGH FOLLOW UP IT WAS LEARNT THAT THE SURGEON IS KEY OPINION LEADER (KOL) FOR SYNERGY IOL PRODUCT AND ALSO AN ARK MYOPIA SPECIALIST. FOR YOUNGER PATIENTS, HE CONSISTENTLY CHOOSES SYNERGY IOLS FOR SURGERY. THIS WAS AN OCCASIONAL CASE OF DIOPTER OR TARGET ERROR IN MULTIFOCAL PROCEDURES. NEVERTHELESS, EVEN IN THIS EXCHANGE SURGERY, HE HAS CONTINUED TO USE SYNERGY IOL. CURRENTLY, HIS SURGICAL OUTCOMES ARE VERY POSITIVE. NO FURTHER INFORMATION IS AVAILABLE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1747963 TECNIS IOL LENS, MULTIFOCAL INTRAOCULAR MFK AMO PUERTO RICO MFG. INC. ZFW150 05050474715776

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Required Intervention