FDA Adverse Event Injury Summary report: N

ACRYSOF RESTOR

MDR report key: 846880 · Received May 9, 2007

Report

Report Number
1119421-2007-00174
Event Type
Injury
Date Received
May 9, 2007
Date of Event
March 16, 2007
Report Date
April 9, 2007
Manufacturer
ALCON LABORATORIES, INC. / HUNGTINGTON
Product Code
HQL
PMA / PMN Number
P040020
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE PRODUCT WAS NOT RETURNED FOR ANALYSIS. STERILIZATION RECORDS WERE REVIEWED AND THE STERILIZATION CYCLE RAN WITHIN ALL REQUIRED PARAMETERS WITH NO ANOMALIES. PRODUCT HISTORY RECORD AND BATCH 060676 RECORDS WERE REVIEWED LENS MET RELEASE CRITERIA. THERE HAVE BEEN NO OTHER COMPLAINTS FOR THIS LOT NUMBER. THIS REPORT WAS MAILED TO THE FDA ON: 05/09/2007. ADDITIONAL INFORMATION WAS REQUESTED 04/09/2007, 04/10/2007, 04/16/2007, 04/20/2007 AND 04/26/2007 BY PHONE, MAIL AND FAX. ADDITIONAL INFORMATION WAS PROVIDED 04/16/2007 AND 04/18/2007 BY MAIL.

Description of Event or Problem · 1

A SURGEON REPORTED FOUR PATIENTS EXPERIENCED TOXIC ANTERIOR SEGMENT SYNDROME (TASS) FOLLOWING INTRAOCULAR LENS (IOL) IMPLANT SURGERIES. SURGERIES OCCURED OVER A THREE WEEK PERIOD AND INVOLVED TWO SURGEONS. THIS REPORT IS BEING SUBMITTED AS MANUFACTURER NUMBER 1119421-2007-00174. THE OTHER MANUFACTURER REPORT NUMBERS ARE MDR #S: 1119421-2007-00172, 1119421-2007-00173, 1119421-2007-00175. NO PRODUCT, PROCEDURAL OR ENVIRONMENTAL FACTOR WAS IDENTIFIED AS A CAUSE. A POSSIBLE SITE VISIT IS BEING DISCUSSED WITH THE SURGEON TO ASSIST THE FACILITY IN IDENTIFYING POSSIBLE CONTRIBUTING FACTORS IN THESE CASES OF TASS. ADDITIONAL INFORMATION, INCLUDING PATIENT STATUS, HAS BEEN REQUEST.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ACRYSOF RESTOR INTRAOCULAR LENS HQL ALCON LABORATORIES, INC. / HUNGTINGTON SN60WF 964885

Patients

Seq Age Sex Outcome Treatment
1 67 YR Required Intervention