LIFESCAN EUROPE GMBH
Manufacturer adverse-event records for LIFESCAN EUROPE GMBH 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 · 2013–2026 · thin-book · quiet Death-code · balanced
Death-code intensity
LIFESCAN EUROPE GMBH is quieter on Death-coded events
Death-coded event_type rows are 0 of 5,428 (0.00% · quiet tercile among 434 manufacturers). Absolute volume is thin-book.
What the Death-code reading shows for LIFESCAN EUROPE GMBH
The standout signal for LIFESCAN EUROPE GMBH is Death-code intensity: 0.00% of 5,428 reports (quiet tercile), while absolute volume is thin-book.
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 7 device types, led in this extract by Malfunction at 3,188 (58.7% of event_type total). Peak single-year volume reaches 3,562 reports across 12 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)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.