FDA Adverse Event Injury Summary report: N

VISIAN ICL (IMPLANTABLE COLLAMER LENS)

MDR report key: 2921691 · Received January 15, 2013

Report

Report Number
2023826-2013-00049
Event Type
Injury
Date Received
January 15, 2013
Date of Event
October 25, 2012
Report Date
December 24, 2012
Manufacturer
STAAR SURGICAL COMPANY
Product Code
MTA
PMA / PMN Number
P030016
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

(B)(4).

Description of Event or Problem · 1

THE REPORTER STATED THE SURGEON IMPLANTED AN 12.0MM ICM120V4 IMPLANTABLE COLLAMER LENS IN PT'S LEFT EYE ON (B)(6) 2012. THE LENS WAS EXPLANTED ON 10/25/2012 DUE TO LOW VAULT. THE LENS WAS EXCHANGED FOR A LONGER LENGTH LENS. PT'S LAST VISIT ON (B)(6) 2012, UCVA WAS 20/20. SEE MFR#2023826-2013-00048 FOR RIGHT EYE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
22942 VISIAN ICL (IMPLANTABLE COLLAMER LENS) INTRAOCULAR LENS MTA STAAR SURGICAL COMPANY ICM120V4 NA

Patients

Seq Age Sex Outcome Treatment
1 26 YR Required Intervention