FDA Adverse Event Injury Summary report: N

VISIAN ICL (IMPLANTABLE COLLAMER LENS)

MDR report key: 2153334 · Received June 30, 2011

Report

Report Number
2023826-2011-00592
Event Type
Injury
Date Received
June 30, 2011
Date of Event
June 1, 2011
Report Date
June 2, 2011
Manufacturer
STAAR SURGICAL CO.
Product Code
MTA
PMA / PMN Number
P030016
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AZ, US
Reporter Occupation
NURSE

Narratives

Additional Manufacturer Narrative · 1

(B)(4). EVAL: LENS WORK ORDER SEARCH. RESULTS - A LENS WORK ORDER SEARCH WAS PERFORMED AND NO SIMILAR COMPLAINTS WERE FOUND WITHIN THE SAME WORK ORDER. (B)(4).

Description of Event or Problem · 1

THE REPORTER STATED THE SURGEON IMPLANTED A MICL 12.6MM IMPLANTABLE COLLAMER LENS IN THE PT'S LEFT EYE. LENS WAS REMOVED DUE TO EXCESSIVE VAULTING AND HIGH IOP. THERE WAS SHALLOWING OF THE ANGLE. THE INCISION WAS NOT WIDENED TO REMOVE THE LENS AND NO SUTURE WAS USED. LENS WAS EXCHANGED FOR A SHORTER LENS. SEE MFR'S 2023826-2011-00593 FOR RIGHT EYE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VISIAN ICL (IMPLANTABLE COLLAMER LENS) INTRAOCULAR LENS MTA STAAR SURGICAL CO. MICL12.6 NA

Patients

Seq Age Sex Outcome Treatment
1 39 YR Required Intervention INJECTOR: MODEL MSI-PF, LOT# UNK| CARTRIDGE: MODEL SFC-45 FP, LOT # UNK| FOAM TIP PLUNGER: MODEL UNK, LOT# UNK