Becton, Dickinson & Co. (sparks)
FDA adverse event reports naming Becton, Dickinson & Co. (sparks) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON, DICKINSON & CO. (SPARKS).
- Total reports
- 7,886
- Deaths
- 1
- Injuries
- 60
- Malfunctions
- 7,825
Reports per year
89720
2,06521
1,67822
1,01123
32224
1,05625
85726
Source: FDA adverse event reports by year received, 2020–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Coronavirus Antigen Detection Test System.QKP1,526
- System, Blood CulturingMDB1,197
- Real Time Nucleic Acid Amplification SystemOOI1,088
- System, Test, Automated, Antimicrobial Susceptibility, Short IncubationLON858
- Culture Media, Non-Selective And Non-DifferentialJSG506
- Culture Media, EnrichedKZI395
- Susceptibility Test Powders, AntimycobacterialMJA320
- Reagents, 2019-Novel Coronavirus Nucleic AcidQJR313
- Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical UseLXG261
- Culture Media, Selective And DifferentialJSI154
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Becton, Dickinson & Co. (sparks) automatically
DeviceWatch watches FDA adverse events and recalls for the products you care about, summarizes clinical narratives with AI and alerts you when a safety signal emerges.