Becton Dickinson, S.A.
FDA adverse event reports naming Becton Dickinson, S.A. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON, S.A..
- Total reports
- 8,242
- Deaths
- 3
- Injuries
- 175
- Malfunctions
- 8,063
Reports per year
111
512
515
3116
30617
94318
1,45619
1,08520
1,54621
1,00222
84723
24624
36325
40626
Source: FDA adverse event reports by year received, 2011–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Syringe, PistonFMF4,368
- Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer SystemONB1,895
- Needle, Hypodermic, Single LumenFMI1,272
- Set, I.V. Fluid TransferLHI197
- Saline, Vascular Access FlushNGT154
- Set, Administration, IntravascularFPA144
- Needle, Conduction, Anesthetic (W/Wo Introducer)BSP75
- Powered Laser Surgical Instrument With MicrobeamFractional OutputONG39
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA27
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ23
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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