FDA Adverse Event Malfunction Summary report: N

MICROSTAAR INJECTOR

MDR report key: 1211324 · Received October 22, 2008

Report

Report Number
2023826-2008-01279
Event Type
Malfunction
Date Received
October 22, 2008
Date of Event
August 20, 2008
Report Date
September 23, 2008
Manufacturer
STAAR SURGICAL CO.
Product Code
KYB
PMA / PMN Number
K954600
Removal / Correction Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
SF
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

EVALUATION CODES: CONCLUSION: AN INVESTIGATION WAS OPENED TO EVALUATE A COMPLAINT TREND ASSOCIATED WITH LENS TEARS THAT WAS ORIGINALLY IDENTIFIED IN JUNE 2005. THE DAMAGE TO THE LENS, AS OBSERVED AND PHOTOGRAPHED UPON THE RETURN OF THE LENS TO STAAR, CAN NOT BE DEFINITIVELY AND EXCLUSIVELY CORRELATED TO A SPECIFIC ROOT CAUSE. POSSIBLE ROOT CAUSES FOR LENS TEARS INCLUDE BOTH DELIVERY SYSTEM ISSUES, AND POSSIBLE HANDLING ERRORS BY THE CUSTOMER. TO ADDRESS DELIVERY SYSTEM ISSUES, ALL STAGES IN THE MANUFACTURING OF THE INJECTORS AND CARTRIDGES WERE REVIEWED AND REVISED, AS OPPORTUNITIES FOR IMPROVEMENT WERE REVEALED. TO ADDRESS HANDLING ERRORS, ALL INJECTOR/CARTRIDGE DIRECTIONS FOR USE (DFU) HAVE BEEN MODIFIED TO ADD FURTHER CLARIFICATIONS TO INSTRUCT THE USERS IN THE PROPER DELIVERY TECHNIQUES THAT ARE EFFECTIVE, AND MINIMIZE THE POTENTIAL FOR DAMAGING THE LENS.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE SURGEON INSERTED AN AQ2010V THREE PIECE SILICONE LENS, AND A HAPTIC GOT CAUGHT ON THE INJECTOR PLUNGER AND TORE UPON INSERTION. THE LENS WAS REMOVED AND THE BACK UP LENS WAS INSERTED WITHOUT PT INJURY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MICROSTAAR INJECTOR INTRAOCULAR LENS GUIDE KYB STAAR SURGICAL CO. MSI-TM UNK

Patients

Seq Age Sex Outcome Treatment
1 10 YR CARTRIDGE: MODEL AQ CARTRIDGE-FP| LENS: MODEL AQ2010V