Becton Dickinson AND Co.
FDA adverse event reports naming Becton Dickinson AND Co. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON AND CO..
- Total reports
- 7,979
- Deaths
- 0
- Injuries
- 512
- Malfunctions
- 7,421
Reports per year
111
312
113
114
3215
8716
16717
36718
1,25319
1,37220
1,63921
1,53022
1,32723
8224
225
Source: FDA adverse event reports by year received, 2011–2025. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Needle, Hypodermic, Single LumenFMI7,663
- Syringe, PistonFMF159
- Injector, PenNSC37
- Pump, InfusionFRN28
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA23
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ16
- Set, Administration, IntravascularFPA15
- Single Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureFMK10
- Saline, Vascular Access FlushNGT7
- Patient Examination GloveFMC3
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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