PlainHospital

BAXTER HEALTHCARE - MEDINA

Manufacturer adverse-event records for BAXTER HEALTHCARE - MEDINA 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 · 2015–2020 · mid-book · typical Death-code · injury-light

Injury-mix signature

BAXTER HEALTHCARE - MEDINA is lighter on Injury codes

Injury-coded event_type share is 0.4% (injury-light tercile) beside 0.07% Death-coded (typical). Volume band: mid.

What the Injury-mix reading shows for BAXTER HEALTHCARE - MEDINA

The standout signal for BAXTER HEALTHCARE - MEDINA is Injury-mix: 0.4% Injury-coded (injury-light) beside 0.07% Death-coded, on a mid-book footprint.

Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for BAXTER HEALTHCARE - MEDINA. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.

Reports span 1 device type, led in this extract by Malfunction at 11,650 (99.5% of event_type total). Peak single-year volume reaches 5,181 reports across 6 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

11,707
Total Reports
8
Event-type Death
49
Injury Reports
1
Device Types

Event Types

Malfunction 11,650 (99.5%)
Injury 49 (0.4%)
Death 8 (0.1%)

Patient Outcomes

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

11,630 (99.2%)
Other 30 (0.3%)
Required Intervention 23 (0.2%)
R 10 (0.1%)
Death 9 (0.1%)
Life Threatening 9 (0.1%)
Disability 3 (0.0%)
Congenital Anomaly 2 (0.0%)
L 1 (0.0%)
Hospitalization 1 (0.0%)

Devices (1)

Device Reports
Pump, Infusion 11,707

Yearly Trend

15
2015: 1
16
2016: 1
17
2017: 2,658
18
2018: 5,181
19
2019: 3,850
20
2020: 16

Read our methodology - how this data is sourced, computed, and verified.