BAXTER HEALTHCARE - CLEVELAND

Manufacturer adverse-event records for BAXTER HEALTHCARE - CLEVELAND 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 · 2008–2020 · mid-book · elevated Death-code · balanced

Death-code intensity

BAXTER HEALTHCARE - CLEVELAND carries an elevated Death-code share

Death-coded event_type rows are 153 of 9,702 (1.58% · elevated tercile among 443 manufacturers). Absolute volume is mid-book.

What the Death-code reading shows for BAXTER HEALTHCARE - CLEVELAND

The standout signal for BAXTER HEALTHCARE - CLEVELAND is Death-code intensity: 1.58% of 9,702 reports (elevated tercile), while absolute volume is mid-book.

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

Reports span 16 device types, led in this extract by Malfunction at 5,715 (58.9% of event_type total). Peak single-year volume reaches 2,918 reports across 13 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

9,702
Total Reports
153
Event-type Death
3,823
Injury Reports
16
Device Types

Event Types

Malfunction 5,715 (58.9%)
Injury 3,823 (39.4%)
Death 153 (1.6%)
11 (0.1%)

Patient Outcomes

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

5,732 (51.2%)
Hospitalization 2,864 (25.6%)
R 1,358 (12.1%)
Required Intervention 504 (4.5%)
Other 441 (3.9%)
Death 157 (1.4%)
H 116 (1.0%)
O 26 (0.2%)
Congenital Anomaly 2 (0.0%)
Life Threatening 2 (0.0%)

Yearly Trend

08
2008: 1
09
2009: 7
10
2010: 365
11
2011: 1,635
12
2012: 1,045
13
2013: 1,386
14
2014: 1,613
15
2015: 2,918
16
2016: 385
17
2017: 218
18
2018: 63
19
2019: 65
20
2020: 1