Becton Dickinson Gmbh
FDA adverse event reports naming Becton Dickinson Gmbh as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON GMBH.
- Total reports
- 3,991
- Deaths
- 0
- Injuries
- 2
- Malfunctions
- 3,989
Reports per year
210
10121
12622
4623
4024
3,64325
3326
Source: FDA adverse event reports by year received, 2010–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Culture Media, EnrichedKZI2,598
- Lectins And ProtectinsKSI700
- Culture Media, Antimicrobial Susceptibility Test, Excluding Mueller Hinton AgarJSO370
- Culture Media, Selective And Non-DifferentialJSJ111
- Culture Media, Non-Selective And Non-DifferentialJSG71
- Culture Media, Selective And DifferentialJSI48
- Culture Media, Antimicrobial Susceptibility Test, Mueller Hinton Agar/BrothJTZ44
- Culture Media, For Isolation Of Pathogenic NeisseriaJTY31
- Culture Media, Non-Selective And DifferentialJSH14
- Culture Media, Multiple Biochemical TestJSE2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
Monitor Becton Dickinson Gmbh 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.