MAUDE Adverse Event Report: Alcon Research, LLC - Irvine Technology Center CENTURION Vision System (Active Sentry); Unit, phacofragmentation

Catalog Number	8065753057
Medical Device Problem Code	Improper Flow or Infusion (2954)
Health Effect - Clinical Codes	Retinal Tear (2050); Intraocular Pressure Decreased (4468)
Type of Reportable Event	Serious Injury
Event or Problem Description
A customer reported that during the cataract surgery with intraocular implantation, ophthalmic system exhibited irrigation stopped when removing the last nuclear quadrant and patient experienced anterior chamber collapsed and hole in posterior capsule.It is unknown whether the procedure was completed.Outcome of the patient was unknown.This report is pertaining to second of two patients from the same facility.
Additional Manufacturer Narrative
Investigation including root cause analysis is in progress.A supplemental mdr will be filed as necessary in accordance with 21 cfr 803.56 when additional reportable information becomes available.The manufacturer internal reference number is: (b)(4).

• Brand Name: CENTURION Vision System (Active Sentry)
• Common Device Name: Unit, phacofragmentation
• Manufacturer (Section D): Alcon Research, LLC - Irvine Technology Center; 15800 alton parkway; irvine CA 92618
• Manufacturer (Section G): Alcon Research, LLC - Irvine Technology Center; 15800 alton parkway; irvine CA 92618
• Manufacturer Contact: jonathan schlech ; 6201 south freeway; mail stop ab2-6; fort worth, TX 76134 ; +1(800)757-9780
• MDR Report Key: 50144656
• Report Number: 2028159-2026-01230
• Device Sequence Number: 10687208
• Product Code: HQC
• UDI-Device Identifier: 00380657530571
• UDI-Public: (01)00380657530571(17)310330(11)210401(10)13UTEH
• Combination Product (Y/N): N
• Initial Reporter State: GA
• Initial Reporter Country: US
• PMA/510(K) Number: K161794
• 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): 08/05/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Catalogue Number: 8065753057
• Device Lot Number: 13UTEH
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Initial Date Received by Manufacturer: 07/16/2026
• Initial Report FDA Received Date: 08/05/2026
• Date Device Manufactured: 04/01/2021
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown