MAQUET SAS
Manufacturer adverse-event records for MAQUET SAS 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 · 2011–2026 · thin-book · quiet Death-code · injury-light
Volume signature
MAQUET SAS is a thinner MAUDE footprint
MAQUET SAS accounts for 4,501 FDA MAUDE reports (#390 of 434, thin-book tercile). Death-coded event_type share is 0.00% (quiet); Injury share 1.8% (injury-light).
What the volume reading shows for MAQUET SAS
The standout signal for MAQUET SAS is filing volume: 4,501 adverse-event reports in FDA MAUDE (#390 of 434, thin-book). Death-coded event_type share sits at 0.00% (quiet).
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 11 device types, led in this extract by Malfunction at 4,411 (98.0% of event_type total). Peak single-year volume reaches 993 reports across 16 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 (11)
Yearly Trend
Read our methodology - how this data is sourced, computed, and verified.