FDA Adverse Event Malfunction Summary report: N

SEE H-10

MDR report key: 3241499 · Received July 22, 2013

Report

Report Number
2023826-2013-00569
Event Type
Malfunction
Date Received
July 22, 2013
Report Date
June 25, 2013
Manufacturer
STAAR SURGICAL COMPANY
Product Code
HQL
PMA / PMN Number
P880091
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

RESULTS: VISUAL INSPECTION OF THE RETURNED LENS SHOWED EVIDENCE OF A CLEAR SURGICAL RESIDUE, HOWEVER, THERE WAS NO VISIBLE DAMAGE TO THE LENS. (B)(4).

Additional Manufacturer Narrative · 1

BRAND NAME: SILICONE ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIECE FOLDABLE INTRAOCULAR LENS (ELASTIC). CONCLUSION: AN INVESTIGATION OF THE ROOT CAUSES OF LENS TEARS, SIMILAR TO THAT STATED IN THIS CLAIM, WERE ADDRESSED IN A CAPA OPENED, WHICH WAS SUBSEQUENTLY CLOSED. THE CAPA ADDRESSED DELIVERY SYSTEM ISSUES INCLUDING ALL STAGES OF MANUFACTURING OF THE INJECTORS AND CARTRIDGES. PROCESSES WERE REVIEWED AND REVISED AS OPPORTUNITIES FOR IMPROVEMENT WERE REVEALED. THE CAPA ALSO ADDRESSED 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. BASED ON THE COMPLAINT HISTORY AND THE EVALUATION OF THE RETURNED PRODUCT, POSSIBLE ROOT CAUSES FOR LENS TEARS INCLUDE BOTH DELIVERY SYSTEM ISSUES AND HANDLING ERRORS BY THE CUSTOMER. (B)(4).

Description of Event or Problem · 1

IT WAS REPORTED THAT THE AA4203TL SILICONE SINGLE PIECE LENS BROKE INSIDE THE EYE. THE LENS WAS REMOVED WITHOUT ANY PATIENT INJURY. THE CUSTOMER COULD NOT PROVIDE ANY OTHER INFORMATION ON THIS CASE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
341408 SEE H-10 INTRAOCULAR LENS HQL STAAR SURGICAL COMPANY AA4203TL N/A

Patients

Seq Age Sex Outcome Treatment
1