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.

8,706
Total Reports
26
Event-type Death
1,364
Injury Reports
20
Device Types

Event Types

Malfunction 7,316 (84.0%)
Injury 1,364 (15.7%)
Death 26 (0.3%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

4,286 (63.0%)
Other 2,350 (34.6%)
Required Intervention 69 (1.0%)
O 29 (0.4%)
Death 19 (0.3%)
Hospitalization 18 (0.3%)
R 13 (0.2%)
H 7 (0.1%)
D 3 (0.0%)
Congenital Anomaly 3 (0.0%)
L 1 (0.0%)
S 1 (0.0%)
Disability 1 (0.0%)

Yearly Trend

21
2021: 18
22
2022: 76
23
2023: 477
24
2024: 886
25
2025: 724
26
2026: 6,525