SISTEMAS MEDICOS ALARIS S.A. DE C.V.
Manufacturer adverse-event records for SISTEMAS MEDICOS ALARIS S.A. DE C.V. 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 · 2000–2026 · thin-book · typical Death-code · injury-light
Injury-mix signature
SISTEMAS MEDICOS ALARIS S.A. DE C.V. is lighter on Injury codes
Injury-coded event_type share is 0.5% (injury-light tercile) beside 0.17% Death-coded (typical). Volume band: thin.
What the Injury-mix reading shows for SISTEMAS MEDICOS ALARIS S.A. DE C.V.
The standout signal for SISTEMAS MEDICOS ALARIS S.A. DE C.V. is Injury-mix: 0.5% Injury-coded (injury-light) beside 0.17% Death-coded, on a thin-book footprint.
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 10 device types, led in this extract by Malfunction at 6,968 (99.3% of event_type total). Peak single-year volume reaches 3,595 reports across 9 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.