Becton Dickinson IND. Cirurgicas Ltda
FDA adverse event reports naming Becton Dickinson IND. Cirurgicas Ltda as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON IND. CIRURGICAS LTDA.
- Total reports
- 3,231
- Deaths
- 0
- Injuries
- 30
- Malfunctions
- 3,201
Reports per year
416
11017
36218
58119
39920
37721
33522
39223
30224
28025
8926
Source: FDA adverse event reports by year received, 2016–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Syringe, PistonFMF1,676
- Needle, Hypodermic, Single LumenFMI817
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA617
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ53
- Container, SharpsMMK27
- Needle, Aspiration And Injection, DisposableGAA17
- Dispenser, Liquid MedicationKYX11
- Tubes, Gastrointestinal (And Accessories)KNT3
- Container, Liquid Medication, GraduatedKYW2
- Syringe, AntistickMEG2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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