B.braun Surgical Sa
FDA adverse event reports naming B.braun Surgical Sa as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: B.BRAUN SURGICAL SA.
- Total reports
- 3,140
- Deaths
- 9
- Injuries
- 86
- Malfunctions
- 3,036
Reports per year
1414
24115
77916
63017
54818
78719
14120
Source: FDA adverse event reports by year received, 2014–2020. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
- Suture, Absorbable, Synthetic, Polyglycolic AcidGAM1,305
- Suture, Nonabsorbable, Synthetic, PolypropyleneGAW645
- Tissue Adhesive For The Topical Approximation Of SkinMPN391
- Suture, Nonabsorbable, Synthetic, PolyamideGAR219
- Suture, Absorbable, NaturalGAL206
- Suture, Surgical, Absorbable, PolydioxanoneNEW148
- Suture, Nonabsorbable, SilkGAP67
- Suture, Nonabsorbable, Synthetic, PolyethyleneGAT56
- Suture, Recombinant TechnologyNWJ32
- Suture, AbsorbableGAK20
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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