FDA Adverse Event Injury Summary report: N

DUOVISC UNKNOWN

MDR report key: 2452467 · Received February 10, 2012

Report

Report Number
3002037047-2012-00029
Event Type
Injury
Date Received
February 10, 2012
Date of Event
January 11, 2012
Report Date
January 11, 2012
Manufacturer
ALCON - BELGIUM/S.A. ALCON-COUVREUR N.V.
Product Code
LZP
PMA / PMN Number
P840064
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
IL, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

THERE WAS NO SAMPLE PRODUCT RETURNED FOR ANALYSIS. THE BATCH RECORDS COULD NOT BE REVIEWED BECAUSE THE REPORTING FACILITY DID NOT PROVIDE A LOT NUMBER OR ANY IDENTIFICATION TRACEABLE TO THE MANUFACTURING DOCUMENTATION. ADDITIONAL INFORMATION WAS REQUESTED ON 01/12/2012, 01/13/2012, 01/20/2012 AND 01/27/2012 BY PHONE, FAX, AND MAIL. A COMPLETED QUESTIONNAIRE WAS RECEIVED ON 02/08/2012. (B)(4).

Description of Event or Problem · 1

A NURSE REPORTED FOUR PATIENTS EXHIBITING TOXIC ANTERIOR SEGMENT SYNDROME, (TASS) FOLLOWING INTRAOCULAR LENS (IOL) IMPLANT SURGERY. THE SYMPTOMS INCLUDED MORE EXCESSIVE THAN NORMAL INFLAMMATION, FIBRIN COATED IOLS THAT TRACK BACK TO THE WOUND. THERE WAS ONE SURGEON INVOLVED AND THE SURGERIES OCCURRED ON THREE SEPARATE DAYS. ADDITIONAL INFORMATION WAS RECEIVED. THE PATIENT'S SYMPTOMS RESOLVED WITH TREATMENT. THERE WAS NO UNPLANNED SURGICAL INTERVENTION REQUIRED. THERE ARE FOUR MEDICAL DEVICE REPORTS ASSOCIATED WITH THIS EVENT. THIS REPORT IS FOR THE FIRST PATIENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DUOVISC UNKNOWN AID, SURGICAL, VISCOELASTIC LZP ALCON - BELGIUM/S.A. ALCON-COUVREUR N.V. NA UNK

Patients

Seq Age Sex Outcome Treatment
1 79 YR Required Intervention MONARCH C| INFINITI| LIDOCAINE| IOPIDINE| ANCEF| CARBACHOL| I/A STRAIGHT SILICONE TIP| DEXAMETHASONE| INTRAOCULAR LENS| TIMOPTIC| BSS WITH EPINEPHRINE| OZIL TORSIONAL PHACO HANDPIECE