MEDLINE INDUSTRIES, LP
Manufacturer adverse-event records for MEDLINE INDUSTRIES, LP 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 · 2021–2026 · mid-book · typical Death-code · balanced
Volume signature
MEDLINE INDUSTRIES, LP sits mid-pack on MAUDE volume
MEDLINE INDUSTRIES, LP accounts for 8,706 FDA MAUDE reports (#269 of 434, mid-book tercile). Death-coded event_type share is 0.30% (typical); Injury share 15.7% (balanced).
What the volume reading shows for MEDLINE INDUSTRIES, LP
The standout signal for MEDLINE INDUSTRIES, LP is filing volume: 8,706 adverse-event reports in FDA MAUDE (#269 of 434, mid-book). Death-coded event_type share sits at 0.30% (typical).
Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for MEDLINE INDUSTRIES, LP. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.
Reports span 20 device types, led in this extract by Malfunction at 7,316 (84.0% of event_type total). Peak single-year volume reaches 6,525 reports across 6 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.