MMJ SA DE CV (USD)
Manufacturer adverse-event records for MMJ SA DE CV 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 · 2016–2025 · thin-book · elevated Death-code · balanced
Volume signature
MMJ SA DE CV is a thinner MAUDE footprint
MMJ SA DE CV (USD) accounts for 6,502 FDA MAUDE reports (#319 of 434, thin-book tercile). Death-coded event_type share is 1.03% (elevated); Injury share 21.0% (balanced).
What the volume reading shows for MMJ SA DE CV (USD)
The standout signal for MMJ SA DE CV (USD) is filing volume: 6,502 adverse-event reports in FDA MAUDE (#319 of 434, thin-book). Death-coded event_type share sits at 1.03% (elevated).
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 5,070 (78.0% of event_type total). Peak single-year volume reaches 1,409 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.