inforMED
InjuryMFK

CLAREON PANOPTIX TRIFOCAL HYDROPHOBIC INTRAOCULAR LENS

Received Jul 10, 2026

Report 1119421-2026-01443 · MDR key 25778711

Device

Generic name

Lens, Multifocal Intraocular

Model number

CNWTT0

Catalog number

CNWTT0.205

Lot number

15309908

Product problems

  • Adverse Event Without Identified Device or Use Problem

Patient

76 YR · Female

  • Blurred Vision
  • Visual Impairment

Narrative

Description of Event or Problem

A NON HEALTH CARE PROFESSIONAL REPORTED THAT FOLLOWING AN INTRAOCULAR LENS (IOL) IMPLANT PROCEDURE, THE PATIENT HAD POOR VISION. CLINICAL REASON BEING MENTIONED AS MYOPIC SHIFT. THE IOL WAS EXPLANTED AND EXCHANGED WITH AN UNSPECIFIED ATIOL (ADVANCED TECHNOLOGY INTRAOCULAR LENS) IN THE SECONDARY IMPLANT PROCEDURE. ADDITIONAL INFORMATION HAS BEEN REQUESTED AND RECEIVED BY STATING THE PATIENT MISSED TARGET. THERE WAS NO FURTHER IMPACT TO THE PATIENT.

Additional Manufacturer Narrative

A PRODUCT WAS NOT RETURNED FOR ANALYSIS. COMPLAINT HISTORY AND PRODUCT HISTORY RECORDS WERE REVIEWED AND DOCUMENTATION INDICATED THE PRODUCT MET RELEASE CRITERIA. ROOT CAUSE HAS NOT BEEN IDENTIFIED. THE MANUFACTURER INTERNAL REFERENCE NUMBER IS: (B)(4).