B. Braun Surgical, S.A.
FDA adverse event reports naming B. Braun Surgical, S.A. as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: B. BRAUN SURGICAL, S.A..
- Total reports
- 3,719
- Deaths
- 3
- Injuries
- 275
- Malfunctions
- 3,441
Reports per year
313
714
415
118
119
34320
52321
55922
46223
47824
72325
61526
Source: FDA adverse event reports by year received, 2013–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM2,346
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW577
- Suture, Nonabsorbable, Synthetic, PolyamideGAR264
- Suture, Surgical, Absorbable, PolydioxanoneNEW186
- Suture, Nonabsorbable, SilkGAP151
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT72
- Stapler, SurgicalGAG30
- Suture, Recombinant TechnologyNWJ28
- Patch, Pledget And Intracardiac, Petp, Ptfe, PolypropyleneDXZ26
- Wax, BoneMTJ19
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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