ALCON LABORATORIES IRELAND LTD.
Manufacturer adverse-event records for ALCON LABORATORIES IRELAND LTD. come from the U.S. Food & Drug Administration (FDA) MAUDE database via openFDA, refreshed March 2026 - see our methodology. Not medical advice.
FDA MAUDE device safety record · 2005–2026 · mid-book · quiet Death-code · balanced
Death-code intensity
ALCON LABORATORIES IRELAND LTD. is quieter on Death-coded events
Death-coded event_type rows are 0 of 9,170 (0.00% · quiet tercile among 434 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for ALCON LABORATORIES IRELAND LTD.
The standout signal for ALCON LABORATORIES IRELAND LTD. is Death-code intensity: 0.00% of 9,170 reports (quiet tercile), while absolute volume is mid-book.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for ALCON LABORATORIES IRELAND LTD.. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 7 device types, led in this extract by Malfunction at 6,154 (67.1% of event_type total). Peak single-year volume reaches 2,598 reports across 22 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Devices (7)
| Device | Reports |
|---|---|
| Intraocular Lens | 5,401 |
| Lens, Intraocular, Toric Optics | 2,679 |
| Lens, Multifocal Intraocular | 614 |
| Extended Depth Of Focus Intraocular Lens | 466 |
| Excimer Laser System | 5 |
| Lens, Guide, Intraocular | 3 |
| Cannula, Ophthalmic | 2 |
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.