Becton Dickinson Industrias Cirurgicas, Ltda.
FDA adverse event reports naming Becton Dickinson Industrias Cirurgicas, Ltda. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA..
- Total reports
- 1,722
- Deaths
- 0
- Injuries
- 93
- Malfunctions
- 1,629
Reports per year
115
816
9517
23418
25019
20120
13921
17722
11523
20324
18725
11226
Source: FDA adverse event reports by year received, 2015–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ1,570
- Needle, Conduction, Anesthetic (W/Wo Introducer)BSP46
- Needle, Hypodermic, Single LumenFMI36
- Set, Administration, IntravascularFPA29
- Anesthesia Conduction KitCAZ13
- Introducer, CatheterDYB8
- Syringe, PistonFMF6
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA5
- Catheter, Intravascular, DiagnosticDQO3
- Needle, Spinal, Short TermMIA2
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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