MOOG MEDICAL DEVICES GROUP
Manufacturer adverse-event records for MOOG MEDICAL DEVICES GROUP 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 · 2008–2026 · mid-book · typical Death-code · injury-light
Injury-mix signature
MOOG MEDICAL DEVICES GROUP is lighter on Injury codes
Injury-coded event_type share is 0.8% (injury-light tercile) beside 0.24% Death-coded (typical). Volume band: mid.
What the Injury-mix reading shows for MOOG MEDICAL DEVICES GROUP
The standout signal for MOOG MEDICAL DEVICES GROUP is Injury-mix: 0.8% Injury-coded (injury-light) beside 0.24% Death-coded, on a mid-book footprint.
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for MOOG MEDICAL DEVICES GROUP. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 10 device types, led in this extract by Malfunction at 8,926 (97.4% of event_type total). Peak single-year volume reaches 1,203 reports across 19 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 (10)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.