MICROPORT CRM S.R.L.
Manufacturer adverse-event records for MICROPORT CRM S.R.L. 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 · 2017–2026 · thin-book · typical Death-code · injury-light
Volume signature
MICROPORT CRM S.R.L. is a thinner MAUDE footprint
MICROPORT CRM S.R.L. accounts for 4,182 FDA MAUDE reports (#410 of 434, thin-book tercile). Death-coded event_type share is 0.57% (typical); Injury share 5.4% (injury-light).
What the volume reading shows for MICROPORT CRM S.R.L.
The standout signal for MICROPORT CRM S.R.L. is filing volume: 4,182 adverse-event reports in FDA MAUDE (#410 of 434, thin-book). Death-coded event_type share sits at 0.57% (typical).
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 14 device types, led in this extract by Malfunction at 3,931 (94.0% of event_type total). Peak single-year volume reaches 1,048 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 (14)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.