BAUSCH & LOMB INCORPORATED
Manufacturer adverse-event records for BAUSCH & LOMB INCORPORATED 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 · 1996–2026 · thin-book · quiet Death-code · balanced
Volume signature
BAUSCH & LOMB INCORPORATED is a thinner MAUDE footprint
BAUSCH & LOMB INCORPORATED accounts for 4,453 FDA MAUDE reports (#380 of 443, thin-book tercile). Death-coded event_type share is 0.02% (quiet); Injury share 13.1% (balanced).
What the volume reading shows for BAUSCH & LOMB INCORPORATED
The standout signal for BAUSCH & LOMB INCORPORATED is filing volume: 4,453 adverse-event reports in FDA MAUDE (#380 of 443, thin-book). Death-coded event_type share sits at 0.02% (quiet).
As a thinner-book manufacturer, a handful of device families can swing the totals; open the device table rather than reading the company headline alone. Event_type counts are not the same population as Patient Outcomes.
Reports span 20 device types, led in this extract by Malfunction at 3,865 (86.8% of event_type total). Peak single-year volume reaches 2,566 reports across 24 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 (20)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.