VENTEC LIFE SYSTEMS, INC
Manufacturer adverse-event records for VENTEC LIFE SYSTEMS, INC 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 · 2018–2026 · thin-book · typical Death-code · injury-light
Volume signature
VENTEC LIFE SYSTEMS, INC is a thinner MAUDE footprint
VENTEC LIFE SYSTEMS, INC accounts for 5,252 FDA MAUDE reports (#364 of 434, thin-book tercile). Death-coded event_type share is 0.40% (typical); Injury share 3.1% (injury-light).
What the volume reading shows for VENTEC LIFE SYSTEMS, INC
The standout signal for VENTEC LIFE SYSTEMS, INC is filing volume: 5,252 adverse-event reports in FDA MAUDE (#364 of 434, thin-book). Death-coded event_type share sits at 0.40% (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 2 device types, led in this extract by Malfunction at 5,067 (96.5% of event_type total). Peak single-year volume reaches 1,031 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 (2)
| Device | Reports |
|---|---|
| Ventilator, Continuous, Facility Use | 5,251 |
| Pump, Portable, Aspiration (Manual Or Powered) | 1 |
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.