FDA Adverse Event Injury Summary report: N

ACRYSOF IQ PANOPTIX UV ABSORBING TRIFOCAL IOL

MDR report key: 15864715 · Received November 25, 2022

Report

Report Number
1119421-2022-02482
Event Type
Injury
Date Received
November 25, 2022
Report Date
November 25, 2022
Manufacturer
ALCON RESEARCH, LLC - HUNTINGTON
Product Code
MFK
UDI-DI
00380652429719
PMA / PMN Number
P040020
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
003

Narratives

Additional Manufacturer Narrative · 0

A SAMPLE DEVICE WAS NOT RETURNED FOR ANALYSIS. PRODUCT HISTORY RECORDS WERE REVIEWED AND DOCUMENTATION INDICATED THE PRODUCT MET RELEASE CRITERIA. ROOT CAUSE HAS NOT BEEN IDENTIFIED. THERE HAVE BEEN NO OTHER COMPLAINTS REPORTED IN THE LOT NUMBER. THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).

Description of Event or Problem · 0

A NON-HEALTHCARE PROFESSIONAL REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, THE PATIENT EXPERIENCED STARBURST, AND HALOS AROUND LIGHTS. CONSUMER'S DOCTOR DID A LENS EXCHANGE IN BOTH EYES WITH THE COMPANY LENS. DOCTOR DID DO A LASER TREATMENT TO TRY TO HELP BUT IT MADE IT WORSE BOTH EYES. CONSUMER CAN'T DRIVE AT NIGHT BECAUSE OF THE ONCOMING LIGHTS AND ALL THE STARBURSTS AND HALOS, EVERYTHING IS DISTORTED. THERE ARE TWO MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS EVENT. THIS REPORT IS ASSOCIATED WITH THE LEFT EYE. ADDITIONAL INFORMATION WAS REQUESTED AND RECEIVED THAT SYMPTOMS STARTED IMMEDIATELY AFTER SURGERY. HAS SEEN RETINAL SPECIALIST AND FINDINGS WERE NORMAL. USING SPECIAL SUN GLASSES TO FUNCTION INDOORS. HAS LEFT HIS JOB BECAUSE OF DEBILITATING GLARE AND IMPACT ON DAILY LIVING ACTIVITIES. HAS SEEN DIFFERENT SECOND OPINION SURGEONS. HAS BEEN ON VUITY DROPS WITH NO IMPROVEMENT OVER TIME. DOES NOT RECOMMEND IOL EXCHANGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2732134 ACRYSOF IQ PANOPTIX UV ABSORBING TRIFOCAL IOL LENS, MULTIFOCAL MFK ALCON RESEARCH, LLC - HUNTINGTON TFAT00 12720027 00380652429719

Patients

Seq Age Sex Outcome Treatment
1 57 YR Male Other| R