FDA Adverse Event Injury Summary report: N

SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA

MDR report key: 1040286 · Received May 8, 2008

Report

Report Number
2023826-2008-00642
Event Type
Injury
Date Received
May 8, 2008
Date of Event
April 15, 2008
Report Date
April 15, 2008
Manufacturer
STAAR SURGICAL
Product Code
HQL
PMA / PMN Number
P900048
Removal / Correction Number
NA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

EVALUATION: CONCLUSIONS: AN INVESTIGATION WAS OPENED TO EVALUATE A COMPLAINT TREND ASSOCIATED WITH LENS TEARS THAT WAS ORIGINALLY IDENTIFIED IN 2005. 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 MFG 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

THE REPORTER STATED, THAT THE SURGEON WAS INSERTING A THREE PIECE SILICONE LENS MODEL AQ2003V AND A HAPTIC BROKE OFF. THE INCISION WAS ENLARGED TO REMOVE THE LENS AND ANOTHER STAAR LENS WAS PLACED IN THE EYE AND A SUTURE WAS USED TO CLOSE THE INCISION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE FOLDABLE INTRAOCULA INTRAOCULAR LENS HQL STAAR SURGICAL AQ2003V NA

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention INJECTOR MODEL: MSI-PM LOT NUMBER: UNK| CARTRIDGE MODEL: AQ CARTRIDGE-FP