Becton Dickinson & Co (franklin Lakes)
FDA adverse event reports naming Becton Dickinson & Co (franklin Lakes) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON DICKINSON & CO (FRANKLIN LAKES).
- Total reports
- 3,482
- Deaths
- 0
- Injuries
- 49
- Malfunctions
- 3,433
Reports per year
77225
2,71026
Source: FDA adverse event reports by year received, 2025–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA2,407
- Set, Administration, IntravascularFPA632
- Tubes, Vacuum Sample, With AnticoagulantGIM240
- Needle, Hypodermic, Single LumenFMI57
- Container, Specimen, SterileFMH52
- Lymphocyte Separation MediumJCF44
- Blood/Plasma Collection Device For Dna TestingPJE16
- Culture Media, Non-Propagating TransportJSM12
- System, Transport, AerobicJTW10
- Single Use Only Blood Lancet With An Integral Sharps Injury Prevention FeatureFMK9
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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