Becton Dickinson Caribe Ltd.
FDA adverse event reports naming Becton Dickinson Caribe Ltd. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON CARIBE LTD..
- Total reports
- 2,842
- Deaths
- 4
- Injuries
- 150
- Malfunctions
- 2,688
Reports per year
307
308
609
410
115
116
217
918
320
56321
26222
91523
18024
73425
7226
Source: FDA adverse event reports by year received, 2007–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- System, Blood CulturingMDB2,449
- Dna Probe, YeastMLA178
- Needle, Conduction, Anesthetic (W/Wo Introducer)BSP65
- Counter, Differential CellGKZ30
- Susceptibility Test Discs, AntimicrobialJTN23
- Catheter, Suprapubic (And Accessories)KOB23
- Antigens, Nontreponemal, AllGMQ21
- Device, Gas GeneratingKZJ12
- Reagents, Specific, AnalyteMVU12
- Discs, Strips And Reagents, Microorganism DifferentiationJTO6
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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