BECTON DICKINSON GMBH

Manufacturer adverse-event records for BECTON DICKINSON GMBH 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 · thin-book · quiet Death-code · injury-light

Injury-mix signature

BECTON DICKINSON GMBH is lighter on Injury codes

Injury-coded event_type share is 0.1% (injury-light tercile) beside 0.00% Death-coded (quiet). Volume band: thin.

What the Injury-mix reading shows for BECTON DICKINSON GMBH

The standout signal for BECTON DICKINSON GMBH is Injury-mix: 0.1% 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 11 device types, led in this extract by Malfunction at 3,989 (99.9% of event_type total). Peak single-year volume reaches 3,643 reports across 7 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

3,991
Total Reports
0
Event-type Death
2
Injury Reports
11
Device Types

Event Types

Malfunction 3,989 (99.9%)
Injury 2 (0.1%)

Patient Outcomes

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

3,987 (99.9%)
Other 2 (0.1%)
Disability 1 (0.0%)
Hospitalization 1 (0.0%)

Yearly Trend

10
2010: 2
21
2021: 101
22
2022: 126
23
2023: 46
24
2024: 40
25
2025: 3,643
26
2026: 33