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 |