BECTON, DICKINSON & CO., (BD)

Manufacturer adverse-event records for BECTON, DICKINSON & CO., 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 · 2010–2026 · mid-book · quiet Death-code · injury-light

Death-code intensity

BECTON, DICKINSON & CO., is quieter on Death-coded events

Death-coded event_type rows are 0 of 12,552 (0.00% · quiet tercile among 434 manufacturers). Absolute volume is mid-book.

What the Death-code reading shows for BECTON, DICKINSON & CO., (BD)

The standout signal for BECTON, DICKINSON & CO., (BD) is Death-code intensity: 0.00% of 12,552 reports (quiet tercile), while absolute volume is mid-book.

Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for BECTON, DICKINSON & CO.,. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.

Reports span 20 device types, led in this extract by Malfunction at 11,775 (93.8% of event_type total). Peak single-year volume reaches 2,168 reports across 14 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

12,552
Total Reports
0
Event-type Death
776
Injury Reports
20
Device Types

Event Types

Malfunction 11,775 (93.8%)
Injury 776 (6.2%)
1 (0.0%)

Patient Outcomes

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

Other 6,134 (48.8%)
5,988 (47.6%)
Required Intervention 413 (3.3%)
R 15 (0.1%)
O 13 (0.1%)
Death 3 (0.0%)
Hospitalization 2 (0.0%)
Life Threatening 1 (0.0%)

Yearly Trend

10
2010: 1
13
2013: 1
15
2015: 7
16
2016: 59
17
2017: 1,188
18
2018: 2,070
19
2019: 2,168
20
2020: 1,027
21
2021: 903
22
2022: 792
23
2023: 953
24
2024: 1,377
25
2025: 2,003
26
2026: 3