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
- 1,188
- Deaths
- 13
- Injuries
- 68
- Malfunctions
- 1,104
Reports per year
107
208
109
313
422
20123
42424
38825
16426
Source: FDA adverse event reports by year received, 2007–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Pump, InfusionFRN794
- Pump, Infusion, ElastomericMEB191
- Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 DaysFOZ75
- Pump, Infusion, PcaMEA50
- Epidural Anesthesia KitOGE34
- Needle, Spinal, Short TermMIA12
- Catheter, Conduction, AnestheticBSO7
- Needle, Conduction, Anesthetic (W/Wo Introducer)BSP6
- Introducer, CatheterDYB6
- Set, Administration, IntravascularFPA5
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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