Becton, Dickinson & Co. (broken Bow)
FDA adverse event reports naming Becton, Dickinson & Co. (broken Bow) as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BECTON, DICKINSON & CO. (BROKEN BOW).
- Total reports
- 9,916
- Deaths
- 0
- Injuries
- 74
- Malfunctions
- 9,842
Reports per year
118
2,23019
1,34220
1,10821
84722
1,32823
1,37724
1,68225
126
Source: FDA adverse event reports by year received, 2018–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Tubes, Vials, Systems, Serum Separators, Blood CollectionJKA7,859
- Tubes, Vacuum Sample, With AnticoagulantGIM857
- Blood/Plasma Collection Device For Dna TestingPJE490
- Culture Media, Non-Propagating TransportJSM202
- Lymphocyte Separation MediumJCF193
- Container, Specimen Mailer And Storage, SterileKDT111
- Container, Specimen, SterileFMH104
- System, Transport, AerobicJTW90
- Culture Media, Anaerobic TransportJSL4
- Syringe, PistonFMF1
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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