MPRI
Manufacturer adverse-event records for MPRI 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 · 2005–2025 · heavy-book · elevated Death-code · injury-heavy
Volume signature
MPRI sits in the heavy MAUDE book
MPRI accounts for 293,149 FDA MAUDE reports (#10 of 443, heavy-book tercile). Death-coded event_type share is 1.85% (elevated); Injury share 56.4% (injury-heavy).
What the volume reading shows for MPRI
The standout signal for MPRI is filing volume: 293,149 adverse-event reports in FDA MAUDE (#10 of 443, heavy-book). Death-coded event_type share sits at 1.85% (elevated).
As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair MPRI with device-family pages before treating company totals as a safety verdict. Event_type Death and Injury are one code per report; Patient Outcomes below use a separate FDA population.
Reports span 20 device types, led in this extract by Injury at 165,354 (56.4% of event_type total). Peak single-year volume reaches 36,491 reports across 21 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.