BAXTER HEALTHCARE - MALTA

Manufacturer adverse-event records for BAXTER HEALTHCARE - MALTA 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 · 2009–2019 · thin-book · quiet Death-code · injury-light

Injury-mix signature

BAXTER HEALTHCARE - MALTA is lighter on Injury codes

Injury-coded event_type share is 0.4% (injury-light tercile) beside 0.00% Death-coded (quiet). Volume band: thin.

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

The standout signal for BAXTER HEALTHCARE - MALTA is Injury-mix: 0.4% Injury-coded (injury-light) beside 0.00% 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 16 device types, led in this extract by Malfunction at 4,258 (99.4% of event_type total). Peak single-year volume reaches 1,081 reports across 11 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

4,282
Total Reports
0
Event-type Death
19
Injury Reports
16
Device Types

Event Types

Malfunction 4,258 (99.4%)
Injury 19 (0.4%)
5 (0.1%)

Patient Outcomes

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

4,261 (99.5%)
Other 10 (0.2%)
Required Intervention 9 (0.2%)
Hospitalization 2 (0.0%)
O 1 (0.0%)
R 1 (0.0%)

Yearly Trend

09
2009: 1
10
2010: 209
11
2011: 829
12
2012: 1,081
13
2013: 637
14
2014: 473
15
2015: 553
16
2016: 243
17
2017: 112
18
2018: 75
19
2019: 69