IPG MFG SWITZERLAND
Manufacturer adverse-event records for IPG MFG SWITZERLAND 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 · 2009–2019 · mid-book · elevated Death-code · injury-heavy
Death-code intensity
IPG MFG SWITZERLAND carries an elevated Death-code share
Death-coded event_type rows are 361 of 18,340 (1.97% · elevated tercile among 443 manufacturers). Absolute volume is mid-book.
What the Death-code reading shows for IPG MFG SWITZERLAND
The standout signal for IPG MFG SWITZERLAND is Death-code intensity: 1.97% of 18,340 reports (elevated tercile), while absolute volume is mid-book.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for IPG MFG SWITZERLAND. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 17 device types, led in this extract by Injury at 10,167 (55.4% of event_type total). Peak single-year volume reaches 7,491 reports across 11 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 (17)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.