Biotronik Ag, Buelach, Switzerland
FDA adverse event reports naming Biotronik Ag, Buelach, Switzerland as the device manufacturer, with recall history from the live FDA recall database. Reporter-supplied name as filed: BIOTRONIK AG, BUELACH, SWITZERLAND.
- Total reports
- 3,561
- Deaths
- 103
- Injuries
- 191
- Malfunctions
- 3,267
Reports per year
53219
61720
62821
56922
55923
47624
18025
Source: FDA adverse event reports by year received, 2019–2025. 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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