BAXTER HEALTHCARE - AIBONITO

Manufacturer adverse-event records for BAXTER HEALTHCARE - AIBONITO 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 · 2009–2020 · thin-book · typical Death-code · injury-light

Injury-mix signature

BAXTER HEALTHCARE - AIBONITO is lighter on Injury codes

Injury-coded event_type share is 3.2% (injury-light tercile) beside 0.15% Death-coded (typical). Volume band: thin.

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

The standout signal for BAXTER HEALTHCARE - AIBONITO is Injury-mix: 3.2% Injury-coded (injury-light) beside 0.15% Death-coded, on a thin-book footprint.

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 13 device types, led in this extract by Malfunction at 7,006 (96.4% of event_type total). Peak single-year volume reaches 1,497 reports across 12 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

7,264
Total Reports
11
Event-type Death
235
Injury Reports
13
Device Types

Event Types

Malfunction 7,006 (96.4%)
Injury 235 (3.2%)
12 (0.2%)
Death 11 (0.2%)

Patient Outcomes

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

7,015 (96.2%)
Required Intervention 104 (1.4%)
Other 88 (1.2%)
Hospitalization 43 (0.6%)
R 22 (0.3%)
Death 11 (0.2%)
O 3 (0.0%)
Life Threatening 3 (0.0%)
H 1 (0.0%)
L 1 (0.0%)

Yearly Trend

09
2009: 28
10
2010: 303
11
2011: 857
12
2012: 1,497
13
2013: 886
14
2014: 883
15
2015: 1,446
16
2016: 607
17
2017: 373
18
2018: 190
19
2019: 193
20
2020: 1