Braun Gmbh Werk Marktheidenfeld
FDA adverse event reports naming Braun Gmbh Werk Marktheidenfeld as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BRAUN GMBH WERK MARKTHEIDENFELD.
- Total reports
- 4,164
- Deaths
- 0
- Injuries
- 50
- Malfunctions
- 4,088
Reports per year
312
2113
3114
40815
48716
44117
31218
23219
24120
31721
13822
45623
48524
46425
12126
Source: FDA adverse event reports by year received, 2012–2026. Reporting paused during the 2026 MAUDE-to-AEMS transition and has since resumed.
Top device categories
Recent recalls
No recalls listed in the FDA device recall database for this entry.
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