Clareon CCW0T4 (UDI 00380652432795)Recalls & reported problems
Alcon Laboratories, Inc. · CLAREON TORIC UVA · Class 3 · Implant
All models of Clareon (1142)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00380652432795), received between Mar 4, 2024 and Mar 4, 2024 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Fibrosis1
- Unspecified Eye / Vision Problem1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 4, 2024Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
A PHYSICIAN REPORTED THAT PATIENT HAD 2+ CELL AND FIBRIN IN ANTERIOR CHAMBER WITH GOOD VISION, NO PAIN, NO REDNESS AND WAS TREATED WITH STEROIDS. ADDITIONAL INFORMATION HAS BEEN REQUESTED, RECEIVED AND STATED THAT POST-OP DAY 1 THE PATIENT HAD MORE INFLAMMATION THAN USUAL WITHOUT SIGNS OF INFECTION, NO PAIN, HAS GOOD VISION, NO VITREOUS CELLS, NO INJECTION. AQUEOUS CELL 2+ AND AQUEOUS FIBRIN PRESENT. THE PATIENT HAD BLEPHARITIS. TOPICAL MEDICATION ADJUSTMENT WAS DONE. NO CULTURES TAKEN. THIS REPORT IS ASSOCIATED WITH MULTIPLE COMPLAINTS. THIS FILE IS 3 OF 3.
Patient problems: Fibrosis; Unspecified Eye / Vision Problem
MAUDE report 18823969 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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