MAUDE Adverse Event Report: Alcon Research, LLC - Huntington Clareon Toric UV Absorbing IOL; Lens, Intraocular, Toric Optics

Model Number	CCW0T6
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/16/2026
Type of Reportable Event	Malfunction
Event or Problem Description
An account manager reported that during an intraocular lens (iol) implant procedure, haptic fell off when the tech was loading the lens.The procedure was completed on the same day.There was no patient contact and no patient harm.
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.A photo was provided.The photo showed a clear, single-piece lens on the outer well of a lens case base.Viscoelastic was visible on the lens.One haptic was broken-gusset area.The broken haptic was visible to the right of the lens.The manufacturer internal reference number is: (b)(4).

• Brand Name: Clareon Toric UV Absorbing IOL
• Common Device Name: Lens, Intraocular, Toric Optics
• Manufacturer (Section D): Alcon Research, LLC - Huntington; 246 kyle lane; huntington WV 25702
• Manufacturer (Section G): Alcon Research, LLC - Huntington; 246 kyle lane; huntington WV 25702
• Manufacturer Contact: jonathan schlech ; 6201 south freeway; mail stop ab2-6; fort worth, TX 76134 ; +1(800)757-9780
• MDR Report Key: 50208298
• Report Number: 1119421-2026-01679
• Device Sequence Number: 10274641
• Product Code: MJP
• UDI-Device Identifier: 00380652435093
• UDI-Public: (01)00380652435093(17)270411(11)230413(10)15618131
• Combination Product (Y/N): N
• Initial Reporter State: OH
• Initial Reporter Country: US
• PMA/510(K) Number: P190018
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 08/11/2026

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: CCW0T6
• Device Catalogue Number: CCW0T6.240
• Device Lot Number: 15618131
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Received by Manufacturer: 07/17/2026
• Initial Report FDA Received Date: 08/11/2026
• Date Device Manufactured: 04/13/2023
• 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
• Concomitant Medical Products and Therapy/Usage Dates: Unspecified Handpiece; Unspecified cartridge
• Patient Sex: Unknown