BAXTER INTERNATIONAL INC.

Manufacturer adverse-event records for BAXTER INTERNATIONAL 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 · 2001–2026 · thin-book · typical Death-code · injury-light

Volume signature

BAXTER INTERNATIONAL INC. is a thinner MAUDE footprint

BAXTER INTERNATIONAL INC. accounts for 4,909 FDA MAUDE reports (#377 of 434, thin-book tercile). Death-coded event_type share is 0.18% (typical); Injury share 1.8% (injury-light).

What the volume reading shows for BAXTER INTERNATIONAL INC.

The standout signal for BAXTER INTERNATIONAL INC. is filing volume: 4,909 adverse-event reports in FDA MAUDE (#377 of 434, thin-book). Death-coded event_type share sits at 0.18% (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 20 device types, led in this extract by Malfunction at 4,809 (98.0% of event_type total). Peak single-year volume reaches 3,868 reports across 14 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

4,909
Total Reports
9
Event-type Death
87
Injury Reports
20
Device Types

Event Types

Malfunction 4,809 (98.0%)
Injury 87 (1.8%)
Death 9 (0.2%)
No answer provided 2 (0.0%)
1 (0.0%)
Other 1 (0.0%)

Patient Outcomes

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

4,718 (95.6%)
Other 123 (2.5%)
Required Intervention 37 (0.7%)
Life Threatening 14 (0.3%)
R 13 (0.3%)
Death 9 (0.2%)
Hospitalization 8 (0.2%)
L 4 (0.1%)
D 3 (0.1%)
H 3 (0.1%)
O 2 (0.0%)

Yearly Trend

01
2001: 1
06
2006: 1
14
2014: 1
16
2016: 5
17
2017: 23
18
2018: 30
19
2019: 11
20
2020: 24
21
2021: 70
22
2022: 164
23
2023: 437
24
2024: 3,868
25
2025: 251
26
2026: 23