BECTON DICKINSON, S.A.

Manufacturer adverse-event records for BECTON DICKINSON, S.A. 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 · 2011–2026 · mid-book · quiet Death-code · injury-light

Injury-mix signature

BECTON DICKINSON, S.A. is lighter on Injury codes

Injury-coded event_type share is 2.1% (injury-light tercile) beside 0.04% Death-coded (quiet). Volume band: mid.

What the Injury-mix reading shows for BECTON DICKINSON, S.A.

The standout signal for BECTON DICKINSON, S.A. is Injury-mix: 2.1% Injury-coded (injury-light) beside 0.04% Death-coded, on a mid-book footprint.

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

Reports span 20 device types, led in this extract by Malfunction at 7,823 (97.8% of event_type total). Peak single-year volume reaches 1,546 reports across 14 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

7,998
Total Reports
3
Event-type Death
171
Injury Reports
20
Device Types

Event Types

Malfunction 7,823 (97.8%)
Injury 171 (2.1%)
Death 3 (0.0%)
Other 1 (0.0%)

Patient Outcomes

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

4,310 (54.2%)
Other 3,540 (44.5%)
Required Intervention 96 (1.2%)
Death 7 (0.1%)
Disability 2 (0.0%)
O 1 (0.0%)
R 1 (0.0%)
Hospitalization 1 (0.0%)
Life Threatening 1 (0.0%)

Yearly Trend

11
2011: 1
12
2012: 5
15
2015: 5
16
2016: 31
17
2017: 306
18
2018: 943
19
2019: 1,456
20
2020: 1,085
21
2021: 1,546
22
2022: 1,002
23
2023: 847
24
2024: 246
25
2025: 363
26
2026: 162