FDA Adverse Event Injury Summary report: N

ACRYSOF TORIC

MDR report key: 3308479 · Received August 19, 2013

Report

Report Number
1119421-2013-00874
Event Type
Injury
Date Received
August 19, 2013
Report Date
July 22, 2013
Manufacturer
ALCON RESEARCH LTD./ HUNTINGTON
Product Code
HQL
PMA / PMN Number
P930014
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
PO
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

EVALUATION SUMMARY: THE PRODUCT WAS NOT RETURNED FOR ANALYSIS. THE PRODUCT HISTORY RECORD COULD NOT BE REVIEWED BECAUSE THE REPORTING FACILITY DID NOT PROVIDE A LOT NUMBER OR ANY IDENTIFICATION TRACEABLE TO THE MANUFACTURING DOCUMENTATION. THE PRODUCT INVESTIGATION COULD NOT IDENTIFY A ROOT CAUSE. NOT ENOUGH INFORMATION WAS PROVIDED FROM THE ACCOUNT FOR FURTHER INVESTIGATION. ADDITIONAL INFO COULD NOT BE OBTAINED, AS THE ARTICLE DID NOT PROVIDE CONTACT INFO FOR THE AUTHOR. CITATION: TIAGO B. FERREIRA, EDUARDO F. MARQUES, ANTONIO RODRIGUES, ROBERT MONTES-MICO. VISUAL AND OPTICAL OUTCOMES OF A DIFFRACTIVE MULTIFOCAL TORIC INTRAOCULAR LENS J CATARACT REFRACT SURG 2013; 39:1029-1035. (B)(4).

Description of Event or Problem · 1

THE AUTHOR OF A LITERATURE ARTICLE REPORTED THAT FOLLOWING A BILATERAL INTRAOCULAR LENS (IOL) IMPLANT SURGERY, A PT PRESENTED WITH A SCORE OF THREE (3) FOR GLARE AND HALOS. THE PT HAD "CONSIDERABLE TROUBLE" AS A RESULT. THE PURPOSE OF THE ARTICLE WAS TO EVALUATE THE OUTCOMES OF PT FOLLOWING TORIC INTRAOCULAR LENS (IOL) IMPLANTATION. NO FURTHER INFO IS EXPECTED. THERE ARE THREE MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS ARTICLE. THIS REPORT IS FOR THE BILATERALLY IMPLANTED PT, RIGHT EYE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
400207 ACRYSOF TORIC INTRAOCULAR LENS HQL ALCON RESEARCH LTD./ HUNTINGTON UNK UNK

Patients

Seq Age Sex Outcome Treatment
1 Other MONARCH III HANDPIECE