KARL STORZ SE & CO. KG
Manufacturer adverse-event records for KARL STORZ SE & CO. KG 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 · 2017–2026 · thin-book · typical Death-code · balanced
Volume signature
KARL STORZ SE & CO. KG is a thinner MAUDE footprint
KARL STORZ SE & CO. KG accounts for 5,916 FDA MAUDE reports (#339 of 434, thin-book tercile). Death-coded event_type share is 0.71% (typical); Injury share 29.9% (balanced).
What the volume reading shows for KARL STORZ SE & CO. KG
The standout signal for KARL STORZ SE & CO. KG is filing volume: 5,916 adverse-event reports in FDA MAUDE (#339 of 434, thin-book). Death-coded event_type share sits at 0.71% (typical).
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 4,100 (69.3% of event_type total). Peak single-year volume reaches 2,394 reports across 10 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.