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
- 6,251
- Deaths
- 0
- Injuries
- 12
- Malfunctions
- 6,239
Reports per year
43923
79724
4,48625
52926
Source: FDA adverse event reports by year received, 2023–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Blood CulturingMDB1,512
- System, Test, Automated, Antimicrobial Susceptibility, Short IncubationLON1,356
- Equipment, Laboratory, General Purpose, Labeled Or Promoted For A Specific Medical UseLXG1,003
- Susceptibility Test Powders, AntimycobacterialMJA527
- Culture Media, Selective And Non-DifferentialJSJ312
- General Purpose ReagentPPM223
- Culture Media, Non-Selective And Non-DifferentialJSG209
- Culture Media, EnrichedKZI141
- Stains, MicrobiologicJTS132
- Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton AgarJSO127
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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