BECTON DICKINSON & CO (FRANKLIN LAKES)

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 · 2025–2026 · thin-book · quiet Death-code · injury-light

Volume signature

BECTON DICKINSON & CO is a thinner MAUDE footprint

BECTON DICKINSON & CO (FRANKLIN LAKES) accounts for 3,814 FDA MAUDE reports (#429 of 434, thin-book tercile). Death-coded event_type share is 0.00% (quiet); Injury share 1.8% (injury-light).

What the volume reading shows for BECTON DICKINSON & CO (FRANKLIN LAKES)

The standout signal for BECTON DICKINSON & CO (FRANKLIN LAKES) is filing volume: 3,814 adverse-event reports in FDA MAUDE (#429 of 434, thin-book). Death-coded event_type share sits at 0.00% (quiet).

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 13 device types, led in this extract by Malfunction at 3,745 (98.2% of event_type total). Peak single-year volume reaches 3,042 reports across 2 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

3,814
Total Reports
0
Event-type Death
69
Injury Reports
13
Device Types

Event Types

Malfunction 3,745 (98.2%)
Injury 69 (1.8%)

Patient Outcomes

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

3,621 (98.3%)
Other 57 (1.5%)
Required Intervention 5 (0.1%)

Yearly Trend

25
2025: 772
26
2026: 3,042