ETHICON ENDO-SURGERY - ALB
Manufacturer adverse-event records for ETHICON ENDO-SURGERY - ALB 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 · 1998–2003 · thin-book · elevated Death-code · balanced
Volume signature
ETHICON ENDO-SURGERY - ALB is a thinner MAUDE footprint
ETHICON ENDO-SURGERY - ALB accounts for 4,470 FDA MAUDE reports (#391 of 434, thin-book tercile). Death-coded event_type share is 0.81% (elevated); Injury share 11.7% (balanced).
What the volume reading shows for ETHICON ENDO-SURGERY - ALB
The standout signal for ETHICON ENDO-SURGERY - ALB is filing volume: 4,470 adverse-event reports in FDA MAUDE (#391 of 434, thin-book). Death-coded event_type share sits at 0.81% (elevated).
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 8 device types, led in this extract by Malfunction at 3,882 (86.8% of event_type total). Peak single-year volume reaches 1,660 reports across 6 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 (8)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.