B. Braun Melsungen Ag
FDA adverse event reports naming B. Braun Melsungen Ag as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: B. BRAUN MELSUNGEN AG.
- Total reports
- 5,922
- Deaths
- 72
- Injuries
- 374
- Malfunctions
- 5,396
Reports per year
24312
65813
60714
57015
64316
26717
28818
58219
28620
25021
24622
31123
35724
35625
15026
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused twice in 2026 during FDA reporting-system changes and has since resumed.
Top device categories
- Pump, InfusionFRN2,823
- Pump, Infusion, ElastomericMEB1,387
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ702
- Epidural Anesthesia KitOGE175
- Cannula, CatheterDQR153
- Set, Administration, IntravascularFPA134
- Introducer, CatheterDYB98
- Syringe, PistonFMF79
- Catheter, Conduction, AnestheticBSO65
- Pump, Infusion, PcaMEA63
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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