FDA Adverse Event Malfunction Summary report: N

IMPLANTABLE COLLAMER LENS (ICL)

MDR report key: 15740188 · Received November 4, 2022

Report

Report Number
2023826-2022-03866
Event Type
Malfunction
Date Received
November 4, 2022
Date of Event
August 11, 2022
Report Date
October 5, 2022
Manufacturer
STAAR SURGICAL COMPANY
Product Code
MTA
PMA / PMN Number
P030016
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
KS
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

(B)(4). CLAIM #(B)(4).

Description of Event or Problem · 0

THE REPORTER INDICATED THAT A 12.6MM VICM5 12.6 OF -8.50 DIOPTER IMPLANTABLE COLLAMER LENS TORE/BROKE DURING LOADING ON (B)(6)2022 . THE LENS WAS NOT IMPLANTED INTO THE PATIENTS RIGHT EYE (OD). A REPLACEMENT LENS OF THE SAME MODEL/SIZE AND DIOPTER WAS IMPLANTED ON THE SAME DAY BUT DIFFERENT SURGERY. THE PROBLEM WAS RESOLVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2212296 IMPLANTABLE COLLAMER LENS (ICL) PHAKIC INTRAOCULAR LENS MTA STAAR SURGICAL COMPANY VICM5 12.6 NA

Patients

Seq Age Sex Outcome Treatment
1 20 YR Female CARTRIDGE MODEL: SFC-45: LOT# 1573939| FOAM TIP PLUNGER (FTP), LOT# 1583653| INJECTOR MODEL: MSI-PF, LOT# UNK