MAUDE Adverse Event Report: ALCON LABORATORIES IRELAND LTD. CLAREON TORIC ASPHERIC HYDROPHOBIC ACRYLIC IOL WITH AUTONOME DELIVERY SYSTEM; LENS, INTRAOCULAR, TORIC OPTICS

Model Number	CNA0T3
Medical Device Problem Code	Material Discolored (1170)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	03/13/2025
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The product was not returned for analysis; the lens remains implanted.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).H.10 reflects all related report numbers associated with this product event that have been submitted at this time.
Event or Problem Description
A physician reported that during a cataract surgery with an intraocular lens (iol) implant procedure, the iol looked blue immediately after the lens was implanted.The surgery was completed without product replacement.It was unknown whether these findings disappeared or continued.The lens remained implanted.There have been no reported health problems or harm to the patient.Additional information was requested, but no further information is available.There are 224 medical device reports associated with this event.This is 178 of 224.
Additional Manufacturer Narrative
Additional information was provided in h.11.The product was not returned for analysis.The root cause could not be determined for the reported anomaly that the lens appeared ¿blue¿ after implant.The issue was not reported at the time the surgery occurred; the initial reporter retroactively reported intraocular lenses from their surgical book.This covered a three-month period from january through march 2025.This was a bulk complaint return involving products manufactured at two different alcon manufacturing sites.By having two different manufacturing sites with different production timelines, the complaints are not considered to be associated with a single, site-specific manufacturing factor.A photo or video confirming the individual complaints was not provided.The surgery was completed without product replacement.Based on the results from the product history record, the products met release criteria.The manufacturer internal reference number is: (b)(4).H.10 reflects all related report numbers associated with this product event that have been submitted at this time.

• Brand Name: CLAREON TORIC ASPHERIC HYDROPHOBIC ACRYLIC IOL WITH AUTONOME DELIVERY SYSTEM
• Common Device Name: LENS, INTRAOCULAR, TORIC OPTICS
• Manufacturer (Section D): ALCON LABORATORIES IRELAND LTD.; cork business&technology park; model farm road; cork 00000 ; EI 00000
• Manufacturer (Section G): ALCON LABORATORIES IRELAND LTD.; cork business&technology park; model farm road; cork 00000 ; EI 00000
• Manufacturer Contact: jonathan schlech ; 6201 south freeway; mail stop ab2-6; fort worth, TX 76134 ; 8007579780
• MDR Report Key: 21928608
• Report Number: 9612169-2025-00900
• Device Sequence Number: 9031008
• Product Code: MJP
• UDI-Device Identifier: 00380652398862
• UDI-Public: (01)00380652398862(17)280624(11)240626(10)25875239
• Combination Product (Y/N): N
• Initial Reporter Country: JA
• PMA/510(K) Number: P190018
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2025
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 07/09/2025

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: CNA0T3
• Device Lot Number: 25875239
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 04/06/2025
• Supplement Date Received by Manufacturer: 06/24/2025
• Initial Report FDA Received Date: 04/29/2025
• Supplement Report FDA Received Date: 07/09/2025
• Date Device Manufactured: 06/26/2024
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1
• Patient Sex: Unknown