BECTON, DICKINSON & CO. (SPARKS)

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 · 2020–2026 · mid-book · quiet Death-code · injury-light

Injury-mix signature

BECTON, DICKINSON & CO. is lighter on Injury codes

Injury-coded event_type share is 0.8% (injury-light tercile) beside 0.01% Death-coded (quiet). Volume band: mid.

What the Injury-mix reading shows for BECTON, DICKINSON & CO. (SPARKS)

The standout signal for BECTON, DICKINSON & CO. (SPARKS) is Injury-mix: 0.8% Injury-coded (injury-light) beside 0.01% 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 & 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 7,037 (99.1% of event_type total). Peak single-year volume reaches 2,065 reports across 7 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

7,098
Total Reports
1
Event-type Death
60
Injury Reports
20
Device Types

Event Types

Malfunction 7,037 (99.1%)
Injury 60 (0.8%)
Death 1 (0.0%)

Patient Outcomes

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

6,611 (93.4%)
Other 426 (6.0%)
Required Intervention 37 (0.5%)
Death 1 (0.0%)

Yearly Trend

20
2020: 897
21
2021: 2,065
22
2022: 1,678
23
2023: 1,011
24
2024: 322
25
2025: 1,056
26
2026: 69