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
- 1,132
- Deaths
- 4
- Injuries
- 1
- Malfunctions
- 1,120
Reports per year
104
6613
61714
41715
3118
Source: FDA adverse event reports by year received, 2004–2018. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM468
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW338
- Suture, Absorbable, NaturalGAL77
- Suture, Surgical, Absorbable, PolydioxanoneNEW62
- Suture, Nonabsorbable, Synthetic, PolyamideGAR49
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT49
- Tissue Adhesive For The Topical Approximation Of SkinMPN20
- Mesh, Surgical, PolymericFTL17
- Suture, Recombinant TechnologyNWJ13
- Suture, Nonabsorbable, Steel, Monofilament And Multifilament, SterileGAQ11
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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