IMPLANTABLE COLLAMER LENS (ICL)
Report
- Report Number
- 2023826-2021-01047
- Event Type
- Malfunction
- Date Received
- April 13, 2021
- Report Date
- March 14, 2021
- Manufacturer
- STAAR SURGICAL COMPANY
- Product Code
- MTA
- PMA / PMN Number
- NA
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- CA
- Reporter Occupation
- PHYSICIAN
- Health Professional
- Yes
Narratives
H6: DEVICE HISTORY RECORD (OHR) REVIEW: BASED ON THE RESULTS OF THE INVESTIGATION, ALL RELEASED DEVICES FROM THE ASSOCIATED WORK ORDER(S), INCLUDING THE SUSPECTED DEVICE; HAVE BEEN MANUFACTURED WITHIN ESTABLISHED PROCESS PARAMETERS; AND THERE IS NO INDICATION THAT THE MANUFACTURING AND PROCESSING OF THE DEVICE CONTRIBUTED TO THE COMPLAINT ISSUE. CLAIM# (B)(4).
B5: PER UPDATED INFORMATION " THE PATIENT IS NOTICING AN IMPROVEMENT IN THEIR SYMPTOMS AND IS HOLDING OFF ON MAKING A DECISION UNTIL WINTER." CLAIM # (B)(4).
THIS PRODUCT IS NOT MARKETED IN THE US. ONE SIMILAR COMPLAINT TYPE EVENTS FOUND WITHIN THE ASSOCIATED LOT. (B)(4).
THE REPORTER INDICATED THAT A 13.2MM, VICM5_13.2, -6.00 DIOPTER, IMPLANTABLE COLLAMER LENS WAS IMPLANTED INTO THE PATIENTS RIGHT EYE (OD) ON (B)(6) 2020. PATIENT IS EXPERIENCING GLARE/HALOES, BLURRED VISION, CIRCLES IN VISION AND RAINBOW HALOES. LENS REMAINS IMPLANTED. THE REPORTER STATED " I BELIEVE HE IS GOING TO WAIT A COUPLE OF MONTHS AND SEE IF HE CAN ADAPT TO THE LENSES." IF ADDITIONAL INFORMATION IS RECEIVED A SUPPLEMENTAL MEDWATCH REPORT WILL BE SUBMITTED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 559208 | IMPLANTABLE COLLAMER LENS (ICL) | PHAKIC INTRAOCULAR LENS | MTA | STAAR SURGICAL COMPANY | VICM5 13.2 | NA |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Male | CARTRIDGE MODEL: SFC-45 W/FTP, LOT# 1456746.| INJECTOR MODEL: MSI-PF, LOT# 1490025. |