FDA Adverse Event Injury Summary report: N

1-DAY ACUVUE TRUEYE (NARAFILCON B)

MDR report key: 3480793 · Received November 8, 2013

Report

Report Number
1033553-2013-00125
Event Type
Injury
Date Received
November 8, 2013
Report Date
November 11, 2013
Manufacturer
VISTAKON
Product Code
LPL
PMA / PMN Number
K100349
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

TWO SEALED BLISTER (S) WERE RETURNED. THE LENSES MEET COMPANY STANDARDS FOR BASE CURVE, CENTER THICKNESS AND DIAMETER. NO OTHER VISUAL ATTRIBUTES OBSERVED. THE SOLUTION WAS TESTED; PH WAS IN SPECIFICATION; THERE WAS NOT ENOUGH SOLUTION TO MEASURE FOR CONDUCTIVITY. A DHR WAS PERFORMED. LOT # 5327580938-OS WAS PROCESSED UNDER NORMAL MANUFACTURING CONDITIONS. THE BATCH RECORD DID NOT SHOW ANY ABNORMALITIES IN MONOMER AND SOLUTION TESTING. ALL PARAMETERS TESTED WERE WITHIN SPECIFICATION. ALL STERILIZATION REQUIREMENTS WERE SUCCESSFULLY COMPLETED. IF ADDITIONAL INFO IS RECEIVED, WILL REPORT WITHIN 30 DAYS OF RECEIPT. MDR REPORTABLE EVENT TRENDS ARE REVIEWED IN QUARTERLY MANAGEMENT REVIEW MEETINGS.

Description of Event or Problem · 1

ON (B)(6) 2013, AN OPTOMETRIST'S OFFICE INFORMED OUR FIRM OF A PT (PT) WHO REPORTED HAVING BEEN DIAGNOSED WITH A CORNEAL ULCER AND TREATED BY AN OPHTHALMOLOGIST. SHE WAS WEARING ACUVUE TRU-EYE CONTACT LENSES (CL) WHEN THE INJURY OCCURRED. ON (B)(6) 2013 OUR FIRM SPOKE WITH THE PT WHO STATED SHE WEARS HER GLASSES MOST OF THE TIME AND ONLY WEARS HER CONTACTS FOR SOCIAL EVENTS. THE PT WAS SEEN BY HER PRIMARY CARE PHYSICIAN WHO TOLD HER SHE THOUGHT SHE HAD "IRITIS". THE PT WAS REFERRED TO AN OPHTHALMOLOGIST AND DIAGNOSED WITH CORNEAL ULCERS OU, OS MORE SEVERE THAN OD. THE PT WAS TREATED WITH ZYMAXID Q2 X3 DAYS THEN QID, ERYTHROMYCIN HS X 7 DAYS AND LOTEMAX (TITRATED) X7 DAYS. ON (B)(6) 2013, THE TREATING OPHTHALMOLOGIST'S OFFICE STATED THE PT WAS DIAGNOSED WITH MARGINAL CORNEAL ULCERS OU. OUR FIRM HAS MADE NUMEROUS UNSUCCESSFUL ATTEMPTS TO COLLECT ADDITIONAL INFO. THE PRECISE NATURE OF THE REPORTED INJURY IS UNK. THIS IS BEING REPORTED AS WORST CASE. MDR #1033553-2013-00124 SUBMITTED FOR THE OD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
578746 1-DAY ACUVUE TRUEYE (NARAFILCON B) SOFT CONTACT LENS LPL VISTAKON NA 5327580938

Patients

Seq Age Sex Outcome Treatment
1 23 YR Required Intervention